Anospec C060110
Anospec C060110 is a Class II device made by Obp Corporation, cleared under FDA 510(k) K121604 on 27 Jul 2012 and listed in FDA GUDID since 21 Sep 2016 (UDI-DI M648C0601100), 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 | NumberM648C0601100 | Date21 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK121604 | Date27 Jul 2012 | StatusActive |
Official records
- FDA 510(k) database K121604
Across registries
- FDA 510(k) K121604 decided 27 Jul 2012 Active
- FDA GUDID UDI-DI M648C0601100 listed 21 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K121604
- Listed FDA GUDID M648C0601100
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Anospec
- Generic name
- Optical anoscope, single-use
- Model / Ref / Catalog
- C060110
- Primary DI / UDI-DI
- M648C0601100
- 510(k) Number
- FDA product code
- FER
- GMDN term
- Optical anoscope, single-use
- Device class
- Class II
- Regulation number
- 876.1500
- GUDID distribution status
- In Commercial Distribution
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