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FDA 510(k)

M.R. ASSOC. SNARES; CRESCENT SNARE WIRE

K-Number: K800965 · 1980-05-08

ApplicantMr Associates, Inc.
Decision Date1980-05-08
Product CodeKNS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

M.R. ASSOC. SNARES; CRESCENT SNARE WIRE is the device name listed in this FDA 510(k) record. The listed applicant is Mr Associates, Inc.. It received FDA 510(k) clearance on 1980-05-08 under 510(k) number K800965. 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 M.R. ASSOC. SNARES; CRESCENT SNARE WIRE?

M.R. ASSOC. SNARES; CRESCENT SNARE WIRE is a medical device that received FDA 510(k) clearance on 1980-05-08. The listed applicant is Mr Associates, Inc.. The 510(k) number is K800965.

When did M.R. ASSOC. SNARES; CRESCENT SNARE WIRE receive FDA 510(k) clearance?

M.R. ASSOC. SNARES; CRESCENT SNARE WIRE received FDA 510(k) clearance on 1980-05-08, under 510(k) number K800965.

Who is the listed applicant for M.R. ASSOC. SNARES; CRESCENT SNARE WIRE?

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

What is the FDA product code for M.R. ASSOC. SNARES; CRESCENT SNARE WIRE?

The FDA product code for M.R. ASSOC. SNARES; CRESCENT SNARE WIRE is KNS.

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Other records listing Mr Associates, Inc. as applicant

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.

K800975M.R. ASSOC. TRUE-FEEL HANDLEK800973M.R. ASSOC. HOT BIOPSY FORCEPSK800974M.R. ASSOC. POWER CORDK800967M.R. ASSOC. ALLIGATOR GRASPONG FORCEPSK800962M.R. ASSOC. WASHING TUBE/MEASURING TUBEK800969M.R. ASSOC. CANNULAS

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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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