Avanos Pmp-145-N

by Avanos Medical, Inc.

Avanos Pmp-145-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 00193493303960), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

FDA submission, from GUDID

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00193493303960 UDI-DI	Date25 Aug 2020Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK002389	Date23 Oct 2000Decided	StatusActive

Official records

AccessGUDID record UDI-DI 00193493303960
FDA 510(k) database 510(k) number K002389

Across registries

2 registries list this device

FDA 510(k) K002389 decided 23 Oct 2000 Active
FDA GUDID UDI-DI 00193493303960 listed 25 Aug 2020 Listed

Timeline

2 dated events

23 Oct 2000 Cleared FDA 510(k) K002389
25 Aug 2020 Listed FDA GUDID 00193493303960

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: Avanos
Generic name: Percutaneous radio-frequency ablation probe, denervation, monopolar, reusable
Model / Ref / Catalog: PMP-145-N

Primary DI / UDI-DI: 00193493303960
510(k) Number: K002389
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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Properties

Lot / batch number
Expiration date

Other properties (13, all answered No)