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Airos A800P

by Airos Medical Inc

Airos A800P is a sequential venous compression system inflator (FDA Class II; FDA product code JOW, Sleeve, Limb, Compressible) made by Airos Medical Inc, listed in FDA GUDID since 18 Jan 2023 (UDI-DI 00850031012011), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850031012011 UDI-DI Date18 Jan 2023ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Airos
Generic name
Sequential venous compression system inflator
Model / reference
A800P
Primary DI / UDI-DI
00850031012011
FDA product code
JOW
GMDN term
Sequential venous compression system inflator
Device class
Class II
Regulation number
870.5800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Sequential venous compression system inflator

Similar devices in this category

Other devices filed under Sequential venous compression system inflator.

Other devices from Airos Medical Inc

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Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)