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FDA 510(k)

COOPERSURGICAL INFRARED COAGULATOR

K-Number: K974168 · 1998-01-23

ApplicantHogan & Hartson
Decision Date1998-01-23
Product CodeKNS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

COOPERSURGICAL INFRARED COAGULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Hogan & Hartson. It received FDA 510(k) clearance on 1998-01-23 under 510(k) number K974168. 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 COOPERSURGICAL INFRARED COAGULATOR?

COOPERSURGICAL INFRARED COAGULATOR is a medical device that received FDA 510(k) clearance on 1998-01-23. The listed applicant is Hogan & Hartson. The 510(k) number is K974168.

When did COOPERSURGICAL INFRARED COAGULATOR receive FDA 510(k) clearance?

COOPERSURGICAL INFRARED COAGULATOR received FDA 510(k) clearance on 1998-01-23, under 510(k) number K974168.

Who is the listed applicant for COOPERSURGICAL INFRARED COAGULATOR?

The FDA 510(k) record lists Hogan & Hartson as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COOPERSURGICAL INFRARED COAGULATOR?

The FDA product code for COOPERSURGICAL INFRARED COAGULATOR is KNS.

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Other records listing Hogan & Hartson 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.

K973849BIOABSORBABLE BANKART TACKK973162DUAL RADIATION TARGETING SYSTEM DRTS DRAPEK950169RIBOSOMAL P EIA TEST SYSTEMK942389TROCARS, TROCAR SLEEVES AND REDUCTION SLEEVESK946217CARDIOLIPIN M EIA TEST SYSTEMK946215CARDIOLIPIN G EIA TEST SYSTEM

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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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