Bovie CS-103LED
by Aspen Surgical Products, Inc. 2 variants
Bovie CS-103LED, a colposcope (FDA Class II; FDA product code HEX, Colposcope (And Colpomicroscope)) made by Aspen Surgical Products, Inc., was cleared under FDA 510(k) K073053 on 15 Nov 2007 and listed in FDA GUDID on 29 Aug 2016 (UDI-DI 10607151011229); the registry lists it as not in commercial distribution (GUDID) 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 | Number10607151011229 | Date29 Aug 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK073053 | Date15 Nov 2007 | StatusActive |
Official records
- AccessGUDID record 10607151011229
- FDA 510(k) database K073053
Across registries
- FDA 510(k) K073053 decided 15 Nov 2007 Active
- FDA GUDID UDI-DI 10607151011229 listed 29 Aug 2016 Listed
Timeline
- Cleared FDA 510(k) K073053
- Listed FDA GUDID 10607151011229
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Bovie
- Generic name
- Colposcope
- Model / Ref / Catalog
- CS-103LED
- Primary DI / UDI-DI
- 10607151011229
- 510(k) Number
- FDA product code
- HEX
- GMDN term
- Colposcope
- Device class
- Class II
- Regulation number
- 884.1630
- GUDID distribution status
- Not in Commercial Distribution
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