Cleared Traditional

SOVIS OPTIQUE'S ENDOSCOPIC CABLE

K023633 · Sovis Optique · Gastroenterology & Urology
Dec 2002
Decision
63d
Days
Class 2
Risk

About This 510(k) Submission

K023633 is an FDA 510(k) clearance for the SOVIS OPTIQUE'S ENDOSCOPIC CABLE, a Image, Illumination, Fiberoptic, For Endoscope (Class II — Special Controls, product code FFS), submitted by Sovis Optique (Washington, US). The FDA issued a Cleared decision on December 31, 2002, 63 days after receiving the submission on October 29, 2002. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.1500.

Submission Details

510(k) Number K023633 FDA.gov
FDA Decision Cleared SESE
Date Received October 29, 2002
Decision Date December 31, 2002
Days to Decision 63 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code FFS — Image, Illumination, Fiberoptic, For Endoscope
Device Class Class II — Special Controls
CFR Regulation 21 CFR 876.1500

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