Skip to content

Setmark Incorporated WC-101

by Setmark Inc.

Setmark Incorporated WC-101 is a wheelchair (FDA Class I; FDA product code IOR, Wheelchair, Mechanical) made by Setmark Inc., cleared under FDA 510(k) K973418 on 9 Oct 1997 and listed in FDA GUDID since 31 Jan 2018 (UDI-DI 00854204008054), 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) K973418

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 Number00854204008054 UDI-DI Date31 Jan 2018ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK973418 Date9 Oct 1997DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K973418 decided 9 Oct 1997 Active
  • FDA GUDID UDI-DI 00854204008054 listed 31 Jan 2018 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K973418
  2. Listed FDA GUDID 00854204008054

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Setmark Incorporated
Generic name
Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible
Model / reference
WC-101
Description
All Stainless Steel W/C, 18' width, removable full length arm, fixed footrest, dark blue#125, rem. front rigging -
Primary DI / UDI-DI
00854204008054
510(k) Number
FDA product code
IOR
GMDN term
Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible
Device class
Class I
Regulation number
890.3850
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Related devices

Category: Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible

Cleared under the same submission (K973418)

and 8 more cleared under K973418

Similar devices

Other devices filed under FDA product code IOR (Wheelchair, Mechanical).

Other devices from Setmark Inc.

See all devices from Setmark Inc. →

Properties

  • Lot / batch number
  • Serial number
Other properties (13, all answered No)