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FDA 510(k)

DIATHERMIC SNARES

K-Number: K820430 · 1982-04-08

ApplicantAmerican Endoscopy, Inc.
Decision Date1982-04-08
Product CodeKNS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DIATHERMIC SNARES is the device name listed in this FDA 510(k) record. The listed applicant is American Endoscopy, Inc.. It received FDA 510(k) clearance on 1982-04-08 under 510(k) number K820430. 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 DIATHERMIC SNARES?

DIATHERMIC SNARES is a medical device that received FDA 510(k) clearance on 1982-04-08. The listed applicant is American Endoscopy, Inc.. The 510(k) number is K820430.

When did DIATHERMIC SNARES receive FDA 510(k) clearance?

DIATHERMIC SNARES received FDA 510(k) clearance on 1982-04-08, under 510(k) number K820430.

Who is the listed applicant for DIATHERMIC SNARES?

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

What is the FDA product code for DIATHERMIC SNARES?

The FDA product code for DIATHERMIC SNARES is KNS.

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Other records listing American Endoscopy, 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.

K853274AMERICAN DILATATION SYSTEMK841384PROXIMA 1 PH MONITORK833491ENDO BITE BLOCKK840818BIOPSY FORCEPSK833859TAMPONADE BALLOON CUFFK833492PERCUTANEOUS ENDOSCOPIC GASTROSCOPY

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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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