Ameda, Inc. 10001
by Ameda, Inc.
Ameda, Inc. 10001 is a Class II device made by Ameda, Inc., cleared under FDA 510(k) K011519 on 15 Aug 2001 and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00810725022856), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None ongoingDocuments
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00810725022856 | Date24 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK011519 | Date15 Aug 2001 | StatusActive |
Official records
- AccessGUDID record 00810725022856
- FDA 510(k) database K011519
Across registries
- FDA 510(k) K011519 decided 15 Aug 2001 Active
- FDA GUDID UDI-DI 00810725022856 listed 24 Sep 2016 Listed
Recalls
-
- Terminated Z-1327-2015
Devices were not sterilized
Timeline
- Cleared FDA 510(k) K011519
- Recall initiated FDA recalls Z-1327-2015
- Listed FDA GUDID 00810725022856
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Ameda, Inc.
- Generic name
- Breast pump support kit, single-use
- Model / Ref / Catalog
- 10001
- Primary DI / UDI-DI
- 00810725022856
- 510(k) Number
- FDA product code
- HGX
- GMDN term
- Breast pump support kit, single-use
- Device class
- Class II
- Regulation number
- 884.5160
- GUDID distribution status
- In Commercial Distribution
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