Halyard 99711
Halyard 99711 (PMP2060C) is a Class II device made by Avanos Medical, Inc., cleared under FDA 510(k) K002389 on 23 Oct 2000 and listed in FDA GUDID since 17 May 2016 (UDI-DI 10680651997118), 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 | Number10680651997118 | Date17 May 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK002389 | Date23 Oct 2000 | StatusActive |
Official records
- AccessGUDID record 10680651997118
- FDA 510(k) database K002389
Across registries
- FDA 510(k) K002389 decided 23 Oct 2000 Active
- FDA GUDID UDI-DI 10680651997118 listed 17 May 2016 Listed
Timeline
- Cleared FDA 510(k) K002389
- Listed FDA GUDID 10680651997118
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Halyard
- Generic name
- Percutaneous radio-frequency ablation probe, denervation, monopolar, reusable
- Model / Ref / Catalog
- 99711, PMP2060C
- Primary DI / UDI-DI
- 10680651997118
- 510(k) Number
- FDA product code
- GXI
- GMDN term
- Percutaneous radio-frequency ablation probe, denervation, monopolar, reusable
- Device class
- Class II
- Regulation number
- 882.4725
- GUDID distribution status
- In Commercial Distribution