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Vasopress

FDA UDI

Class II (US FDA UDI)

by Compression Therapy Concepts

Identity

Trade Name
Vasopress FDA UDI
Generic Name
Intermittent venous compression system pump FDA UDI
Model / Reference
VP500 FDA UDI

Identifiers

Primary DI / UDI-DI
00815245010000 FDA UDI
510(k) Number
K000147 FDA UDI
FDA Product Code
JOW FDA UDI
GMDN Term
Intermittent venous compression system pump FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Intermittent venous compression system pump

Vasopress by Compression Therapy Concepts — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intermittent venous compression system pump.

Cleared under the same submission

K000147 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Compression Therapy Concepts

Sources (1)

  • FDA UDI ee5b7935-c888-48b2-a471-b07aefba402d 34 fields · synced Jun 8, 2026