Cleared Traditional

SONOSURG SYSTEM

K032066 · The Olympus Optical Co. · General & Plastic Surgery
Oct 2003
Decision
92d
Days
Risk

About This 510(k) Submission

K032066 is an FDA 510(k) clearance for the SONOSURG SYSTEM, a Instrument, Ultrasonic Surgical, submitted by The Olympus Optical Co. (Melville, US). The FDA issued a Cleared decision on October 3, 2003, 92 days after receiving the submission on July 3, 2003. This device falls under the General & Plastic Surgery review panel.

Submission Details

510(k) Number K032066 FDA.gov
FDA Decision Cleared SESE
Date Received July 03, 2003
Decision Date October 03, 2003
Days to Decision 92 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code LFL — Instrument, Ultrasonic Surgical
Device Class

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