510(k) K781109

FORCEPS, ELECTROSURGICAL by Kli — Product Code HIN

K781109 is an FDA 510(k) premarket notification submitted by Kli for the device "FORCEPS, ELECTROSURGICAL". The FDA issued a decision of Substantially Equivalent on September 14, 1978. The device falls under product code HIN (Coagulator-Cutter, Endoscopic, Bipolar (And Accessories)), a Class II device regulated under 21 CFR 884.4150. Kli has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 14, 1978
Date Received
June 30, 1978
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Coagulator-Cutter, Endoscopic, Bipolar (And Accessories)
Device Class
Class II
Regulation Number
884.4150
Review Panel
OB
Submission Type