ProKids FM85030-CCM1
ProKids FM85030-CCM1 is a Class II device made by Prestige Ameritech, cleared under FDA 510(k) K160100 on 7 Oct 2016 and listed in FDA GUDID since 26 Sep 2016 (UDI-DI 00852212003269), 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 | FDA 510(k)SESE | NumberK160100 | Date7 Oct 2016 | StatusActive |
| United States | GUDID listing | Number00852212003269 | Date26 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 00852212003269
- FDA 510(k) database K160100
Across registries
- FDA 510(k) K160100 decided 7 Oct 2016 Active
- FDA GUDID UDI-DI 00852212003269 listed 26 Sep 2016 Listed
Timeline
- Listed FDA GUDID 00852212003269
- Cleared FDA 510(k) K160100
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- ProKids
- Generic name
- Surgical/medical face mask, non-antimicrobial, single-use
- Model / reference
- FM85030-CCM1
- Primary DI / UDI-DI
- 00852212003269
- 510(k) Number
- FDA product code
- OXZ
- GMDN term
- Surgical/medical face mask, non-antimicrobial, single-use
- Device class
- Class II
- Regulation number
- 878.4040
- GUDID distribution status
- In Commercial Distribution
Similar devices
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