510(k) K943776

COAGULATOR CUTTER, ENDOSCOPIC BIPOLAR AND ACCESSORIES by Richard Wolf Medical Instruments Corp. — Product Code HIN

K943776 is an FDA 510(k) premarket notification submitted by Richard Wolf Medical Instruments Corp. for the device "COAGULATOR CUTTER, ENDOSCOPIC BIPOLAR AND ACCESSORIES". The FDA issued a decision of Substantially Equivalent on November 3, 1994. The device falls under product code HIN (Coagulator-Cutter, Endoscopic, Bipolar (And Accessories)), a Class II device regulated under 21 CFR 884.4150. Richard Wolf Medical Instruments Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 3, 1994
Date Received
August 2, 1994
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