Identity
- Trade Name
- ALP® FDA UDI
- Generic Name
- Intermittent venous compression system pump FDA UDI
- Device Name
- ALP 1A CALF-R - Garment (Calf, Adult) FDA UDI
- Model / Reference
- ALP® 1A CALF-R FDA UDI
- Description
- ALP 1A CALF-R - Garment (Calf, Adult) FDA UDI
Identifiers
- Catalog Number
- 500003 FDA UDI
- Primary DI / UDI-DI
- 00857910006017 FDA UDI
- 510(k) Number
- K955853 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
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
Yes
FDA UDI
Prescription Use
No
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
Yes
FDA UDI
Category: Intermittent venous compression system pump
Alp® by Cavalier Alp, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
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
- Cavalier Alp, LLC
Sources (1)
- FDA UDI e85bf0a5-378f-415c-8527-8c0af9c457f4 35 fields · synced Jun 8, 2026