510(k) K932293

CABOT MEDICAL BIPOLAR CUTTING FORCEPS by Cabot Medical Corp. — Product Code KNS

K932293 is an FDA 510(k) premarket notification submitted by Cabot Medical Corp. for the device "CABOT MEDICAL BIPOLAR CUTTING FORCEPS". The FDA issued a decision of Substantially Equivalent on July 27, 1994. The device falls under product code KNS (Unit, Electrosurgical, Endoscopic (With Or Without Accessories)), a Class II device regulated under 21 CFR 876.4300. Cabot Medical Corp. has at least 10 other 510(k) clearances on record.