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FDA 510(k)

POLYPECTOMY SNARE

K-Number: K810336 · 1981-03-20

ApplicantMedi-Tech, Inc.
Decision Date1981-03-20
Product CodeKNS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

POLYPECTOMY SNARE is the device name listed in this FDA 510(k) record. The listed applicant is Medi-Tech, Inc.. It received FDA 510(k) clearance on 1981-03-20 under 510(k) number K810336. 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 POLYPECTOMY SNARE?

POLYPECTOMY SNARE is a medical device that received FDA 510(k) clearance on 1981-03-20. The listed applicant is Medi-Tech, Inc.. The 510(k) number is K810336.

When did POLYPECTOMY SNARE receive FDA 510(k) clearance?

POLYPECTOMY SNARE received FDA 510(k) clearance on 1981-03-20, under 510(k) number K810336.

Who is the listed applicant for POLYPECTOMY SNARE?

The FDA 510(k) record lists Medi-Tech, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POLYPECTOMY SNARE?

The FDA product code for POLYPECTOMY SNARE is KNS.

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Other records listing Medi-Tech, Inc. as applicant

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K954457MEDI-TECH EDDY INTRAVASCULAR INFUSION CATHETERK952345MEDI-TECH PLATFORM GUIDE CATHETERK952056IMMUNOASSAY DRUGS OF ABUSE CONTROLSK945289DOA - IMMUNOASSAY CUT-OFF CALIBRATORK942551THERAPEUTIC DRUG MONITORING CONTROL, ASSAYEDK943290BILIRUBIN PLUS/PEDIATRIC CONTROLS

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Related Devices (Code: KNS)

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.

K262460Rezum SystemBoston ScientificK260962SphincterotomeTaewoong Medical Co., Ltd.K252388Vanquish Water Vapor Ablation DeviceFrancis Medical, Inc.K252889Single Use 3-Lumen Needle Knife V (KD-V441M, KD-V451M)Olympus Medical Systems CorporationK250945Single 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.

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