← Back to catalogue

Alp®

FDA UDI

Class II (US FDA UDI)

by Cavalier Alp, LLC

Identity

Trade Name
ALP® FDA UDI
Generic Name
Single-chamber venous compression system garment, single-use FDA UDI
Device Name
ALP® 1PS - Garment (Calf, Pediatric) FDA UDI
Model / Reference
ALP® 1PS FDA UDI
Description
ALP® 1PS - Garment (Calf, Pediatric) FDA UDI

Identifiers

Catalog Number
500018 FDA UDI
Primary DI / UDI-DI
00857910006079 FDA UDI
510(k) Number
K143317 FDA UDI
FDA Product Code
JOW FDA UDI
GMDN Term
Single-chamber venous compression system garment, single-use 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: Single-chamber venous compression system garment, single-use

Alp® by Cavalier Alp, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Single-chamber venous compression system garment, single-use.

Cleared under the same submission

K143317 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Cavalier Alp, LLC

Sources (1)

  • FDA UDI dd9a04a5-703e-47f3-9cd8-c0a736af810d 35 fields · synced Jun 8, 2026