Prosurg NAN23
by Prosurg, Inc
Prosurg NAN23 is a Class II device made by Prosurg, Inc, cleared under FDA 510(k) K152511 on 11 Jul 2016 and listed in FDA GUDID since 12 May 2020 (UDI-DI 00851545007814), 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 | GUDID listing | Number00851545007814 | Date12 May 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK152511 | Date11 Jul 2016 | StatusActive |
Official records
- AccessGUDID record 00851545007814
- FDA 510(k) database K152511
Across registries
- FDA 510(k) K152511 decided 11 Jul 2016 Active
- FDA GUDID UDI-DI 00851545007814 listed 12 May 2020 Listed
Timeline
- Cleared FDA 510(k) K152511
- Listed FDA GUDID 00851545007814
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Prosurg
- Generic name
- Rigid optical arthroscope, single-use
- Model / Ref / Catalog
- NAN23
- Primary DI / UDI-DI
- 00851545007814
- 510(k) Number
- FDA product code
- HRX
- GMDN term
- Rigid optical arthroscope, single-use
- Device class
- Class II
- Regulation number
- 888.1100
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Ethylene Oxide
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