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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® 3 THIGH-R - Garment (Thigh, Adult) FDA UDI
Model / Reference
ALP® 3 THIGH-R FDA UDI
Description
ALP® 3 THIGH-R - Garment (Thigh, Adult) FDA UDI

Identifiers

Catalog Number
500006 FDA UDI
Primary DI / UDI-DI
00857910006093 FDA UDI
510(k) Number
K955853 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

Yes

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

K955853 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cavalier Alp, LLC

Sources (1)

  • FDA UDI 3c63c7eb-21aa-4c99-ab8e-42c51cc0f840 35 fields · synced May 30, 2026