Conmed 60-1769-001

by Conmed Corporation

Conmed 60-1769-001 is a Class II device made by Conmed Corporation, cleared under FDA 510(k) K964176 on 14 Aug 1997 and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 20653405008825), 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	Number20653405008825 UDI-DI	Date24 Sep 2016Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK964176	Date14 Aug 1997Decided	StatusActive

Official records

AccessGUDID record UDI-DI 20653405008825
FDA 510(k) database 510(k) number K964176

Across registries

2 registries list this device

FDA 510(k) K964176 decided 14 Aug 1997 Active
FDA GUDID UDI-DI 20653405008825 listed 24 Sep 2016 Listed

Timeline

2 dated events

14 Aug 1997 Cleared FDA 510(k) K964176
24 Sep 2016 Listed FDA GUDID 20653405008825

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: Conmed
Generic name: Endoscopic electrosurgical electrode, bipolar, reusable
Model / Ref / Catalog: 60-1769-001

Primary DI / UDI-DI: 20653405008825
510(k) Number: K964176
FDA product code: GEI
GMDN term: Endoscopic electrosurgical electrode, bipolar, reusable

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

Sterilisation method: Moist Heat or Steam Sterilization

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

Sterilise before use
Prescription use
Lot / batch number
Manufacturing date

Other properties (11, all answered No)