Drivemedical MQ9120
Drivemedical MQ9120 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 1 Jul 2016 (UDI-DI 00822383542942), active (FDA 510(k)), not in commercial distribution (GUDID) as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00822383542942 | Date1 Jul 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK113315 | Date20 Nov 2012 | StatusActive |
Official records
- AccessGUDID record 00822383542942
- FDA 510(k) database K113315
Across registries
- FDA 510(k) K113315 decided 20 Nov 2012 Active
- FDA GUDID UDI-DI 00822383542942 listed 1 Jul 2016 Listed
Timeline
- Cleared FDA 510(k) K113315
- Listed FDA GUDID 00822383542942
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Drivemedical
- Generic name
- Breast pump, electric
- Model / reference
- MQ9120
- Primary DI / UDI-DI
- 00822383542942
- FDA product code
- HGX
- GMDN term
- Breast pump, electric
- Device class
- Class II
- Regulation number
- 884.5160
- GUDID distribution status
- Not in Commercial Distribution
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