McKesson 179
by Mckesson Medical-Surgical Inc.
McKesson 179 is a colposcope (FDA Class II; FDA product code HEX, Colposcope (And Colpomicroscope)) made by Mckesson Medical-Surgical Inc., cleared under FDA 510(k) K073053 on 15 Nov 2007 and listed in FDA GUDID since 9 Dec 2016 (UDI-DI 40612479200034), 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 | Number40612479200034 | Date9 Dec 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK073053 | Date15 Nov 2007 | StatusActive |
Official records
- AccessGUDID record 40612479200034
- FDA 510(k) database K073053
Across registries
- FDA 510(k) K073053 decided 15 Nov 2007 Active
- FDA GUDID UDI-DI 40612479200034 listed 9 Dec 2016 Listed
Timeline
- Cleared FDA 510(k) K073053
- Listed FDA GUDID 40612479200034
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- McKesson
- Generic name
- Colposcope
- Model / reference
- 179
- Primary DI / UDI-DI
- 40612479200034
- 510(k) Number
- FDA product code
- HEX
- GMDN term
- Colposcope
- Device class
- Class II
- Regulation number
- 884.1630
- GUDID distribution status
- In Commercial Distribution
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