7205611
7205611 is a Class II device made by Smith & Nephew, Inc., cleared under FDA 510(k) K970949 on 23 Apr 1997 and listed in FDA GUDID since 23 Aug 2015 (UDI-DI 00885554009958), 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 | Number00885554009958 | Date23 Aug 2015 | StatusListed |
| United States | FDA 510(k)SESE | NumberK970949 | Date23 Apr 1997 | StatusActive |
Official records
- AccessGUDID record 00885554009958
- FDA 510(k) database K970949
Across registries
- FDA 510(k) K970949 decided 23 Apr 1997 Active
- FDA GUDID UDI-DI 00885554009958 listed 23 Aug 2015 Listed
Timeline
- Cleared FDA 510(k) K970949
- Listed FDA GUDID 00885554009958
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Generic name
- Meniscus forceps
- Model / Ref / Catalog
- 7205611
- Primary DI / UDI-DI
- 00885554009958
- 510(k) Number
- FDA product code
- GCJ
- GMDN term
- Meniscus forceps
- Device class
- Class II
- Regulation number
- 876.1500
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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