FDA 510(k) K140503, FLEXIVA SF SIDE-FIRING SINGLE-USE LASER FIBER, THIRD PARTY REVIEW GROUP, LLC
FDA 510(k) K140503, FLEXIVA SF SIDE-FIRING SINGLE-USE LASER FIBER, THIRD PARTY REVIEW GROUP, LLC
Device Name: FLEXIVA SF SIDE-FIRING SINGLE-USE LASER FIBER
Manufacturer: THIRD PARTY REVIEW GROUP, LLC
Device Classification Name: Powered Laser Surgical Instrument
Regulation Number: 878.4810
Classification Product Code: GEX
Date Received: 02/27/2014
Decision Date: 04/15/2014
Regulation Medical Specialty: General & Plastic Surgery
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