Skip to content

Chair Conversion Kit 36800-CCK

by Accutron

Chair Conversion Kit 36800-CCK is a Class II device made by Accutron, cleared under FDA 510(k) K970163 on 10 Dec 1997 and listed in FDA GUDID since 14 Sep 2023 (UDI-DI 00813830024579), active as of 22 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

510(k) K970163

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00813830024579 UDI-DI Date14 Sep 2023ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK970163 Date10 Dec 1997DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K970163 decided 10 Dec 1997 Active
  • FDA GUDID UDI-DI 00813830024579 listed 14 Sep 2023 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K970163
  2. Listed FDA GUDID 00813830024579

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Chair Conversion Kit
Generic name
Oxygen/air/nitrous oxide breathing gas mixer
Model / Ref / Catalog
36800-CCK
Primary DI / UDI-DI
00813830024579
510(k) Number
FDA product code
BSZ
GMDN term
Oxygen/air/nitrous oxide breathing gas mixer
Device class
Class II
Regulation number
868.5160
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code BSZ (Gas-Machine, Anesthesia).

Other devices from Accutron

See all devices from Accutron →

Properties

  • Prescription use
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)