Cleared Traditional

K990850 - COOPERSURGICAL COAGULATOR FOR TATTOO REMOVAL (FDA 510(k) Clearance)

Jun 1999
Decision
78d
Days
Class 2
Risk

K990850 is an FDA 510(k) clearance for the COOPERSURGICAL COAGULATOR FOR TATTOO REMOVAL. This device is classified as a Unit, Electrosurgical, Endoscopic (with Or Without Accessories) (Class II - Special Controls, product code KNS).

Submitted by CooperSurgical, Inc. (Washington, US). The FDA issued a Cleared decision on June 1, 1999, 78 days after receiving the submission on March 15, 1999.

This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.4300.

Submission Details

510(k) Number K990850 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 15, 1999
Decision Date June 01, 1999
Days to Decision 78 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code KNS — Unit, Electrosurgical, Endoscopic (with Or Without Accessories)
Device Class Class II - Special Controls
CFR Regulation 21 CFR 876.4300

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