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Medquip MQ9000

by Drive Devilbiss Healthcare

Medquip MQ9000 is a Class II device made by Drive Devilbiss Healthcare, cleared under FDA 510(k) K113315 on 20 Nov 2012 and listed in FDA GUDID since 21 Jun 2019 (UDI-DI 00718122644391), active (FDA 510(k)), not in commercial distribution (GUDID) as of 22 Oct 2026.

Active United States. Also listed in GUDID (US), not in commercial distribution.

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) K113315

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 Number00718122644391 UDI-DI Date21 Jun 2019ListedStatusListed GUDID: not in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK113315 Date20 Nov 2012DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K113315 decided 20 Nov 2012 Active
  • FDA GUDID UDI-DI 00718122644391 listed 21 Jun 2019 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K113315
  2. Listed FDA GUDID 00718122644391

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Medquip
Generic name
Breast pump, electric
Model / reference
MQ9000
Primary DI / UDI-DI
00718122644391
FDA product code
HGX
GMDN term
Breast pump, electric
Device class
Class II
Regulation number
884.5160
GUDID distribution status
Not in Commercial Distribution

Related devices

Cleared under the same submission (K113315)

Similar devices

Other devices filed under FDA product code HGX (PUMP, BREAST, POWERED).

Other devices from Drive Devilbiss Healthcare

See all devices from Drive Devilbiss Healthcare →

Properties

  • Over-the-counter
  • Serial number
Other properties (13, all answered No)