FDA.reportPublic FDA data

ThermoTek WRAP, DVT, CALF SET, PUSH, SPU

Primary DI
00850033615272
Brand
ThermoTek WRAP, DVT, CALF SET, PUSH, SPU
Company
THERMOTEK, INC.
Model
0P9BNDVTCA4
Catalog number
0P9BNDVTCA4
Device description
WRAP, DVT, CALF SET, PUSH, SPU
Published
2026-02-21
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Single use
true

Product Codes#

Code, Name table
CodeName
JOWSleeve, Limb, Compressible

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
JOWSleeve, Limb, CompressibleCardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K061866000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K061866000NANOTHERM, VASCUTHERM AND PROTHERMO THERAPY WRAPSThermotek, Inc.2006-08-22JOW

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00850033615272PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00850033615272008500336152728500336152720850033615272

GMDN Terms#

Term, Definition table
TermDefinition
Single-chamber venous compression system garment, single-useAn inflatable device in the form of a stocking, sleeve, or suit intended to be applied to the limbs externally to promote venous blood flow. As part of a compression system, the device applies pressure to the extremities through the intermittent inflation of a single-chamber. The resulting increased venous blood flow may help to treat/prevent oedema, deep vein thrombosis (DVT) and pulmonary embolism (PE) in non-ambulatory patients or patients at risk. This is a single-use device.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
847899911
Device count
1
Lot or batch
true
Manufacturing date on label
true
No natural rubber latex
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00850033615227Echo Ultrasound Device (PRC) 0V52XX1001JK01-CTN0V52XX1001JK01-CTN2026-02-23
00850033615258Echo Ultrasound Device (PRC)0V52XX1001JK010V52XX1001JK012026-02-23
00850033615289Echo Ultrasound Device (USA)0V52XX1002JK01-CTN0V52XX1002JK01-CTN2026-02-23
00850033615340Echo Ultrasound Device (USA)0V52XX1002JK010V52XX1002JK012026-02-23
00850033615371Echo BOX, DRESSING & GEL POD PACK, USND, PRC0V52XX1003JK01 0V52XX1003JK01 2026-02-23
00850033615388Echo CTN, DRESSINGS, USND, PRC, QTY 4 BOXES0V52XX1003JK01-CTN0V52XX1003JK01-CTN2026-02-23
00850033615425Echo Ultra Sound Gel Pods, Carton0V52XX1004JK01-CTN0V52XX1004JK01-CTN2026-02-23
00850033615487Echo Ultra Sound Gel Pod, Single0V52XX1004JK010V52XX1004JK012026-02-23
00850033615500Echo APPLICATOR, SINGLE, USND0V52XX1005JK010V52XX1005JK012026-02-23
00850033615517Echo POWER SUPPLY, CORD, SINGLE, USND0V52XX1006JK010V52XX1006JK012026-02-23
00850033615531Echo BELT CLIP, DEVICE PRTCTR, SNGL,USND0V52XX1007JK010V52XX1007JK012026-02-23
00850033615555Echo ARM STRAP, DEVICE PRTCTR, SNG, USND0V52XX1008JK010V52XX1008JK012026-02-23
00850033615562Echo GEL, TUBE, SINGLE, USND0V52XX1009JK010V52XX1009JK012026-02-23
00850033615586echoRx, MANUAL, USER, SINGLE, USND0V52XX1010JK010V52XX1010JK012026-02-23
00850033615593echoRx, GUIDE,QUICK START,SNGL,USND0V52XX1011JK010V52XX1011JK012026-02-23
00850033615616ThermoTek WRAP, KN/FL, SG GRD,CF,EXT SPU, UF0P9BCFKNMR3EXT-U 0P9BCFKNMR3EXT-U 2026-02-23
00850033615623Echo CTN, DRESSINGS, USND, USA, QTY 4 BOXES0V52XX1012JK01-CTN 0V52XX1012JK01-CTN 2026-02-23
00850033615630Echo BOX, DRESSING & GEL POD PACK, USND, USA0V52XX1012JK010V52XX1012JK012026-02-23
00850033615647THERAPY SYSTEM, ARTEK PRO-020P9PTATP020P9PTATP022026-02-23
00850033615081ThermoTek WRAP, BACK W/BRACE,LSO,ONE-SIZE0P9BLSBXBK0P9BLSBXBK2026-02-21

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Primary DI, Brand, Company table
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10192253057737CARDINAL HEALTHCardinal Health 200, LLCJOW2024-10-02
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