Skip to content

Mabis 01-160-021

by Dms Holdings, Inc.,

Mabis 01-160-021 is a Class II device made by Dms Holdings, Inc.,, cleared under FDA 510(k) K082542 on 17 Sep 2008 and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 00767056160026), active as of 23 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 23 Oct 2026

Documents

510(k) K082542

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00767056160026 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK082542 Date17 Sep 2008DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K082542 decided 17 Sep 2008 Active
  • FDA GUDID UDI-DI 00767056160026 listed 23 Sep 2016 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K082542
  2. Listed FDA GUDID 00767056160026

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Mabis
Generic name
Aneroid manual sphygmomanometer
Model / Ref / Catalog
01-160-021
Primary DI / UDI-DI
00767056160026
FDA product code
DXQ
GMDN term
Aneroid manual sphygmomanometer
Device class
Class II
Regulation number
870.1120
GUDID distribution status
In Commercial Distribution

Related devices

Category: Aneroid manual sphygmomanometer

Cleared under the same submission (K082542)

and 8 more cleared under K082542

Similar devices

Other devices filed under FDA product code DXQ (Blood Pressure Cuff).

Other devices from Dms Holdings, Inc.,

See all devices from Dms Holdings, Inc., →

Properties

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