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Medium Size Oxygen Hood #1547

by Ann Arbor Plastics, Inc.

510(k) K802653

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 10 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 10 Oct 2026. What this means

Regulatory status

as of registry sync 10 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK802653 Date24 Nov 1980ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 10 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
BYL
Device Class
Class I
Regulation
21 CFR Part 868.5700
Advisory Committee
Anesthesiology
FDA Decision
SESE Substantially Equivalent

Other devices from Ann Arbor Plastics, Inc.

  • Oxygen Hoods

    Class I