Identity
- Trade Name
- VasoPress FDA UDI
- Generic Name
- Intermittent venous compression system pump FDA UDI
- Model / Reference
- VP510 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00815245010222 FDA UDI
- 510(k) Number
- K101915 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 5 Feet 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.
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- ALP® — Cavalier Alp, LLC · Class II
- AeroDVx ™ — SUN-SCIENTIFIC INC. · Class II
- Entre — TACTILE SYSTEMS TECHNOLOGY INC · Class II
Cleared under the same submission
K101915 also covers:
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Compression Therapy Concepts
Sources (1)
- FDA UDI 304b3157-a3e8-4f8c-bbb0-4fb0c28f63fc 35 fields · synced Jun 8, 2026