Argent 22-A942

by Mckesson Medical-Surgical Inc.

Argent 22-A942 is a Class II device made by Mckesson Medical-Surgical Inc., cleared under FDA 510(k) K000961 on 19 Apr 2000 and listed in FDA GUDID since 7 Aug 2017 (UDI-DI 20612479212965), 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	Number20612479212965 UDI-DI	Date7 Aug 2017Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Special	NumberK000961	Date19 Apr 2000Decided	StatusActive

Official records

AccessGUDID record UDI-DI 20612479212965
FDA 510(k) database 510(k) number K000961

Across registries

2 registries list this device

FDA 510(k) K000961 decided 19 Apr 2000 Active
FDA GUDID UDI-DI 20612479212965 listed 7 Aug 2017 Listed

Timeline

2 dated events

19 Apr 2000 Cleared FDA 510(k) K000961
7 Aug 2017 Listed FDA GUDID 20612479212965

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: Argent
Generic name: Electrosurgical return electrode, reusable
Model / reference: 22-A942

Primary DI / UDI-DI: 20612479212965
510(k) Number: K000961
FDA product code: GEI
GMDN term: Electrosurgical return electrode, reusable

Device class: Class II
Regulation number: 878.4400
GUDID distribution status: In Commercial Distribution

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Properties

Prescription use
Lot / batch number
Serial number
Manufacturing date

Other properties (11, all answered No)