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FDA 510(k)

COOPERSURGICAL COAGULATOR FOR TATTOO REMOVAL

K-Number: K990850 · 1999-06-01

ApplicantCooperSurgical, Inc.
Decision Date1999-06-01
Product CodeKNS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

COOPERSURGICAL COAGULATOR FOR TATTOO REMOVAL is the device name listed in this FDA 510(k) record. The listed applicant is CooperSurgical, Inc.. It received FDA 510(k) clearance on 1999-06-01 under 510(k) number K990850. 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 COAGULATOR FOR TATTOO REMOVAL?

COOPERSURGICAL COAGULATOR FOR TATTOO REMOVAL is a medical device that received FDA 510(k) clearance on 1999-06-01. The listed applicant is CooperSurgical, Inc.. The 510(k) number is K990850.

When did COOPERSURGICAL COAGULATOR FOR TATTOO REMOVAL receive FDA 510(k) clearance?

COOPERSURGICAL COAGULATOR FOR TATTOO REMOVAL received FDA 510(k) clearance on 1999-06-01, under 510(k) number K990850.

Who is the listed applicant for COOPERSURGICAL COAGULATOR FOR TATTOO REMOVAL?

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

What is the FDA product code for COOPERSURGICAL COAGULATOR FOR TATTOO REMOVAL?

The FDA product code for COOPERSURGICAL COAGULATOR FOR TATTOO REMOVAL is KNS.

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Other records listing CooperSurgical, 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.

K261083Wallace® Aspiration Pump (WAPV1); Wallace® Pump Filter Connector (WFC); Wallace® Vacuum Connection Kit (WVCK)K243799Fetal PillowK250438CooperSurgical Milex® PessariesK223064ALLY II Uterine Positioning System™ (UPS)K201086Advincula Delineator Uterine ManipulatorK200038Endosee 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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