Skip to content

Accu-Vac 56955

by Accutron

Accu-Vac 56955 is a Class II device made by Accutron, cleared under FDA 510(k) K033503 on 12 Mar 2004 and listed in FDA GUDID since 28 Sep 2016 (UDI-DI 00813830023572), 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) K033503

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 Number00813830023572 UDI-DI Date28 Sep 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Special NumberK033503 Date12 Mar 2004DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K033503 decided 12 Mar 2004 Active
  • FDA GUDID UDI-DI 00813830023572 listed 28 Sep 2016 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K033503
  2. Listed FDA GUDID 00813830023572

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Accu-Vac
Generic name
Anaesthesia workstation gas scavenger
Model / Ref / Catalog
56955
Primary DI / UDI-DI
00813830023572
510(k) Number
FDA product code
CBN
GMDN term
Anaesthesia workstation gas scavenger
Device class
Class II
Regulation number
868.5430
GUDID distribution status
In Commercial Distribution

Similar devices in this category

Other devices filed under Anaesthesia workstation gas scavenger.

Other devices from Accutron

See all devices from Accutron →

Properties

  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)