Avanos Pmp-145C-N
Avanos Pmp-145C-N 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 25 Aug 2020 (UDI-DI 00193493303977), 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 | Number00193493303977 | Date25 Aug 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK002389 | Date23 Oct 2000 | StatusActive |
Official records
- AccessGUDID record 00193493303977
- FDA 510(k) database K002389
Across registries
- FDA 510(k) K002389 decided 23 Oct 2000 Active
- FDA GUDID UDI-DI 00193493303977 listed 25 Aug 2020 Listed
Timeline
- Cleared FDA 510(k) K002389
- Listed FDA GUDID 00193493303977
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Avanos
- Generic name
- Percutaneous radio-frequency ablation probe, denervation, monopolar, reusable
- Model / Ref / Catalog
- PMP-145C-N
- Primary DI / UDI-DI
- 00193493303977
- 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
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