FDA.reportPublic FDA data

VascuTrak®

Primary DI
00801741061981
Brand
VascuTrak®
Company
Bard Peripheral Vascular, Inc.
Model
V184060S
Catalog number
V184060S
Device description
VascuTrak® PTA Dilatation Catheter 4 mm x 60 mm, 80 cm catheter
Published
2016-08-18
Public version status
Update
Distribution status
Not in Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
PNOCatheter, percutaneous, cutting/scoring

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
PNOCatheter, Percutaneous, Cutting/ScoringCardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K103459000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K103459000VASCUTRAK PTA DILATATION CATHETERC.R. Bard, Inc.2010-12-13PNO

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00801741061981PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00801741061981008017410619818017410619810801741061981

GMDN Terms#

Term, Definition table
TermDefinition
Peripheral angioplasty balloon catheter, basicA sterile, non-drug-eluting, flexible tube designed for percutaneous transluminal angioplasty (PTA) to dilate a stenotic peripheral (i.e., non-cerebral, non-coronary) artery by controlled inflation of a distensible balloon(s) at its distal tip; it may also be intended for positioning and expansion of a stent/stent-graft. It is available as an over-the-wire (OTW) type with multiple lumens, or a rapid exchange (RX) type with a single lumen. Some types may include cutting/scoring elements (e.g., microsurgical blades, dual wire configurations) to score/modify the plaque. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+1(800)321-4254medical.services@crbard.com

Regulatory Flags#

DUNS number
135057938
Device count
1
Lot or batch
true
Expiration date on label
true
No natural rubber latex
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00801741000331UltraClip® II Breast Tissue Marker8610178610172015-09-25
00801741032004SenoMark® Ultra Breast Tissue MarkerSMEC7CSMEC7C2015-10-02
00801741032011SenoMark® Ultra Breast Tissue MarkerSMEC7RSMEC7R2015-10-02
00801741032028SenoMark® Ultra Breast Tissue MarkerSMEC10CSMEC10C2015-10-01
00801741032035SenoMark® Ultra Breast Tissue MarkerSMEC10RSMEC10R2015-10-01
00801741032042SenoMark® Ultra Breast Tissue MarkerSMEC12CSMEC12C2015-10-01
00801741032059SenoMark® Ultra Breast Tissue MarkerSMEC12RSMEC12R2015-10-02
00801741032066SenoMark® Ultra Breast Tissue MarkerSMMA11CSMMA11C2015-10-01
00801741032073SenoMark® Ultra Breast Tissue MarkerSMMA11RSMMA11R2015-10-01
00801741032080SenoMark® Ultra Breast Tissue MarkerSMAT9CSMAT9C2015-10-02
00801741032097SenoMark® Ultra Breast Tissue MarkerSMAT9RSMAT9R2015-10-02
00801741032103SenoMark® Ultra Breast Tissue MarkerSMAT12CSMAT12C2015-10-01
00801741032110SenoMark® Ultra Breast Tissue MarkerSMAT12RSMAT12R2015-10-01
00801741032127SenoMark® Ultra Breast Tissue MarkerSMEV9CSMEV9C2015-10-02
00801741032134SenoMark® Ultra Breast Tissue MarkerSMEV9RSMEV9R2015-10-02
00801741032219UltraClip® Dual Trigger Breast Tissue Marker862017D862017D2015-09-25
00801741032226UltraClip® Dual Trigger Breast Tissue Marker862017DL862017DL2015-09-25
00801741032233UltraClip® Dual Trigger Breast Tissue Marker863017D863017D2015-09-25
00801741032240UltraClip® Dual Trigger Breast Tissue Marker863017DL863017DL2015-09-25
00801741032257UltraClip® Dual Trigger Breast Tissue Marker864017D864017D2015-09-25

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
06923533801330Peripheral Scoring Balloon Dilatation CatheterDK Medical Technology Co., Ltd.PNO2026-07-30
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06923533801385Peripheral Scoring Balloon Dilatation CatheterDK Medical Technology Co., Ltd.PNO2026-07-30
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06923533801415Peripheral Scoring Balloon Dilatation CatheterDK Medical Technology Co., Ltd.PNO2026-07-30
06923533801422Peripheral Scoring Balloon Dilatation CatheterDK Medical Technology Co., Ltd.PNO2026-07-30
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06923533801460Peripheral Scoring Balloon Dilatation CatheterDK Medical Technology Co., Ltd.PNO2026-07-30
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06923533801491Peripheral Scoring Balloon Dilatation CatheterDK Medical Technology Co., Ltd.PNO2026-07-30
06923533801507Peripheral Scoring Balloon Dilatation CatheterDK Medical Technology Co., Ltd.PNO2026-07-30
06923533801514Peripheral Scoring Balloon Dilatation CatheterDK Medical Technology Co., Ltd.PNO2026-07-30
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06923533801538Peripheral Scoring Balloon Dilatation CatheterDK Medical Technology Co., Ltd.PNO2026-07-30
06923533801545Peripheral Scoring Balloon Dilatation CatheterDK Medical Technology Co., Ltd.PNO2026-07-30
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06923533801620Peripheral Scoring Balloon Dilatation CatheterDK Medical Technology Co., Ltd.PNO2026-07-30