FDA.reportPublic FDA data

CELLO™, Balloon Guide Catheter

Primary DI
04544050093446
Brand
CELLO™, Balloon Guide Catheter
Company
FUJI SYSTEMS CORPORATION
Model
6F
Catalog number
1610560
Device description
The CELLO Balloon Guide Catheter is indicated for use in facilitating the insertion and guidance of intravascular catheters into a selected blood vessel in the peripheral and neuro vasculature systems. The balloon provides temporary vascular occlusion during these and other angiographic procedures.
Published
2015-09-24
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
MR Unsafe
Rx
true
OTC
false
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
DQYCatheter, Percutaneous

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DQYCatheter, PercutaneousCardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K120781000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K120781000CELLO BALLOON GUIDE CATHETER (6F), 950 MM AND 1020 MM LENGTHFuji Systems Corp.2012-08-09DQY

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
04544050093446PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
04544050093446045440500934464544050093446

GMDN Terms#

Term, Definition table
TermDefinition
Vascular guide-catheter, single-useA flexible tube intended to be used for the percutaneous transluminal passage and placement of a diagnostic/interventional catheter, lead (e.g., pacing lead, balloon dilatation catheter), needle or guidewire through its lumen(s), within the vascular system. It may be rigid or flexible, non-steerable or steerable, single or multiple lumen(s), and the distal section can have a variety of preformed shapes. It is not intended solely for infusion nor to access superselective small vessels, and does not include a transseptal needle. A percutaneous introduction set, shaft visualization electrodes, or haemostatic valve may be supplied with the guide-catheter. This is a single-use device.

Contacts#

Phone, Email table
PhoneEmail
949-837-3700XX@XX.XX

Regulatory Flags#

DUNS number
715919973
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
true
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
true
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
04544050093460CELLO™, Balloon Guide Catheter7F16105702015-09-24
04544050093484CELLO™, Balloon Guide Catheter8F16105802015-09-24
04544050093491CELLO™, Balloon Guide Catheter9F16105902015-09-24
04544050121057CELLO II Balloon Guide Catheter, 8F 90cm16509082026-05-25
04544050123815UNIVENT TUBE (TCB TYPE)I.D. 8.0MM12029332024-01-31
04544050123839UNIVENT TUBE (TCB TYPE)I.D. 6.0MM12029272024-01-31
04544050123846UNIVENT TUBE (TCB TYPE)I.D. 6.5MM12029282024-01-31
04544050123853UNIVENT TUBE (TCB TYPE)I.D. 7.0MM12029302024-01-31
04544050123860UNIVENT TUBE (TCB TYPE)I.D. 7.5MM12029312024-01-31
04544050123877UNIVENT TUBE (TCB TYPE)I.D. 8.5MM12029352024-01-31
04544050123884UNIVENT TUBE (TCB TYPE)I.D. 9.0MM12029362024-01-31
04544050123891UNIVENT TUBE (TCB TYPE)I.D. 9.5MM12029372024-01-31
04544050123907UNIVENT TUBE (TCB TYPE)I.D. 10.0MM12029392024-01-31
14544050123812UNIVENT TUBE (TCB TYPE)I.D. 8.0MM12029332024-01-31
14544050123836UNIVENT TUBE (TCB TYPE)I.D. 6.0MM12029272024-01-31
14544050123843UNIVENT TUBE (TCB TYPE)I.D. 6.5MM12029282024-01-31
14544050123850UNIVENT TUBE (TCB TYPE)I.D. 7.0MM12029302024-01-31
14544050123867UNIVENT TUBE (TCB TYPE)I.D. 7.5MM12029312024-01-31
14544050123874UNIVENT TUBE (TCB TYPE)I.D. 8.5MM12029352024-01-31
14544050123881UNIVENT TUBE (TCB TYPE)I.D. 9.0MM12029362024-01-31

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