Ameda, Inc. 17003
by Ameda, Inc.
Ameda, Inc. 17003 is a Class II device made by Ameda, Inc., cleared under FDA 510(k) K950531 on 22 Sep 1995 and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00810725021705), active as of 22 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 | Number00810725021705 | Date24 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK950531 | Date22 Sep 1995 | StatusActive |
Official records
- AccessGUDID record 00810725021705
- FDA 510(k) database K950531
Across registries
- FDA 510(k) K950531 decided 22 Sep 1995 Active
- FDA GUDID UDI-DI 00810725021705 listed 24 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K950531
- Listed FDA GUDID 00810725021705
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Ameda, Inc.
- Generic name
- Breast pump, electric
- Model / Ref / Catalog
- 17003
- Primary DI / UDI-DI
- 00810725021705
- 510(k) Number
- FDA product code
- HGX
- GMDN term
- Breast pump, electric
- Device class
- Class II
- Regulation number
- 884.5160
- GUDID distribution status
- In Commercial Distribution
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