Minncare HD 3029764
Minncare HD 3029764 is a Class II device made by Medivators Inc., cleared under FDA 510(k) K133724 on 27 Aug 2014 and listed in FDA GUDID since 26 Mar 2024 (UDI-DI 00724995223298), active 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 | Number00724995223298 | Date26 Mar 2024 | StatusListed |
| United States | FDA 510(k)SESE | NumberK133724 | Date27 Aug 2014 | StatusActive |
Official records
- AccessGUDID record 00724995223298
- FDA 510(k) database K133724
Across registries
- FDA 510(k) K133724 decided 27 Aug 2014 Active
- FDA GUDID UDI-DI 00724995223298 listed 26 Mar 2024 Listed
Timeline
- Cleared FDA 510(k) K133724
- Listed FDA GUDID 00724995223298
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Minncare HD
- Generic name
- Organic peroxy acid device sterilant, single-use
- Model / Ref / Catalog
- 3029764
- Primary DI / UDI-DI
- 00724995223298
- 510(k) Number
- FDA product code
- NIH
- GMDN term
- Organic peroxy acid device sterilant, single-use
- Device class
- Class II
- Regulation number
- 876.5665
- GUDID distribution status
- In Commercial Distribution