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Golden Power Lift Chair

by Golden Technologies, Inc.

510(k) K880800

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None ongoing

1 closed

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK880800 Date14 Mar 1988ClearedStatusActive

Recalls

1 recall · FDA

    • Terminated Z-2817-2020 FDA Class II initiated 6 Jul 2020

    Suspect poor weld on back KD bar.

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  • Withdrawn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
INO
Device Class
Class II
Regulation
21 CFR Part 890.3110
Advisory Committee
Physical Medicine
FDA Decision
SESE Substantially Equivalent

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