FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CABOT MEDICAL BIPOLAR CUTTING FORCEPS

K Number: K932293 · Decision Jul 27, 1994
Classifications
1
FEI Numbers
117
Registration Numbers
117
Same Product Code
187
Applicant Total
38
Review Days
442

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Basic Information

Device Name
CABOT MEDICAL BIPOLAR CUTTING FORCEPS
K Number
K932293
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.4300
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cabot Medical Corp.
Date Received
May 11, 1993
Decision Date
July 27, 1994
Product Code
KNS
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KNS Unit, Electrosurgical, Endoscopic (With Or Without Accessories)

Similar 510(k) Clearances

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Other Clearances by Cabot Medical Corp.

K Number Device Name
K960148 CIRCON-SURGITEK CLASSIC DOUBLE PIGTAIL URETERAL STENT
K946109 CABOT MEDICAL REUSABLE BIPOLAR CUTTING FORCEPS
K951972 CABOT MEDICAL ULTRA FLOW CYSTOURETHROSCOPE SYSTEM WITH OPERATING & DIAGNOSTIC SHEATHS
K951714 CABOT MEDICAL-SURGITEK ULTRAGOLD PLUS SIDE-FIRING UROLOGIC LASER FIBER
K941743 CABOT MEDICAL NIAGARA FLUID MANAGEMENT PUMP
K934115 3000 ELECTRONIC INSUFFLATOR MODIFICATION
K930954 THE CABOT MEDICAL INSUL-SHETH VAGINAL SPECULUM COV
K932626 CABOT MEDICAL SURGIFLEX(R) SUCTION-IRRIGATION PROB
K935786 CORSON AND NEZHAT SUCTION/IRRIGATION PROBES
K924631 CABOT MEDICAL UTERINE RESECTOSCOPE
Search all 38 clearances from Cabot Medical Corp. →