510(k) K772220

PROBE, COAGULATION ACCESSORY by Kli — Product Code KNF

K772220 is an FDA 510(k) premarket notification submitted by Kli for the device "PROBE, COAGULATION ACCESSORY". The FDA issued a decision of Substantially Equivalent on December 13, 1977. The device falls under product code KNF (Coagulator-Cutter, Endoscopic, Unipolar (And Accessories)), a Class II device regulated under 21 CFR 884.4160. Kli has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 13, 1977
Date Received
December 5, 1977
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Coagulator-Cutter, Endoscopic, Unipolar (And Accessories)
Device Class
Class II
Regulation Number
884.4160
Review Panel
OB
Submission Type