FDA 510(k)

CABOT MEDICAL REUSABLE BIPOLAR CUTTING FORCEPS

K-Number: K946109 · 1995-11-21

Decision Date1995-11-21

Product CodeKNS

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

CABOT MEDICAL REUSABLE BIPOLAR CUTTING FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Cabot Medical Corp.. It received FDA 510(k) clearance on 1995-11-21 under 510(k) number K946109. The device is classified under product code KNS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CABOT MEDICAL REUSABLE BIPOLAR CUTTING FORCEPS?

CABOT MEDICAL REUSABLE BIPOLAR CUTTING FORCEPS is a medical device that received FDA 510(k) clearance on 1995-11-21. The listed applicant is Cabot Medical Corp.. The 510(k) number is K946109.

When did CABOT MEDICAL REUSABLE BIPOLAR CUTTING FORCEPS receive FDA 510(k) clearance?

CABOT MEDICAL REUSABLE BIPOLAR CUTTING FORCEPS received FDA 510(k) clearance on 1995-11-21, under 510(k) number K946109.

Who is the listed applicant for CABOT MEDICAL REUSABLE BIPOLAR CUTTING FORCEPS?

The FDA 510(k) record lists Cabot Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CABOT MEDICAL REUSABLE BIPOLAR CUTTING FORCEPS?

The FDA product code for CABOT MEDICAL REUSABLE BIPOLAR CUTTING FORCEPS is KNS.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Cabot Medical Corp. as applicant

K960148CIRCON-SURGITEK CLASSIC DOUBLE PIGTAIL URETERAL STENT K951972CABOT MEDICAL ULTRA FLOW CYSTOURETHROSCOPE SYSTEM WITH OPERATING & DIAGNOSTIC SHEATHS K951714CABOT MEDICAL-SURGITEK ULTRAGOLD PLUS SIDE-FIRING UROLOGIC LASER FIBER K941743CABOT MEDICAL NIAGARA FLUID MANAGEMENT PUMP K9341153000 ELECTRONIC INSUFFLATOR MODIFICATION K932293CABOT MEDICAL BIPOLAR CUTTING FORCEPS

View all 38 devices →

Related Devices (Code: KNS)

K262460Rezum SystemBoston Scientific K260962SphincterotomeTaewoong Medical Co., Ltd.K252388Vanquish Water Vapor Ablation DeviceFrancis Medical, Inc.K252889Single Use 3-Lumen Needle Knife V (KD-V441M, KD-V451M)Olympus Medical Systems Corporation K250945Single Use Preloaded Sphincterotome V (Distal Wire Guided) (KD-VC600 Series); Single Use Sphincterotome V (Distal Wire Guided) (KD-VC400 Series); Single Use 3-Lumen Sphincterotome (KD-V Series); Disposable Triple Lumen Sphincterotome (KD Series)Olympus Medical Systems Corp.K250351Single Use Electrosurgical Knife (KD-612L, KD-612U); Single Use Electrosurgical Knife (KD-620UR); Single Use Electrosurgical Knife (KD-650L, KD-650U)Olympus Medical Systems Corporation

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.