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FDA 510(k) K160172, Laparoscope Lens Shield Device, by Medeon Biodesign, Inc.

FDA 510(k) K160172, Laparoscope Lens Shield Device, by Medeon Biodesign, Inc.

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510(K) Number: K160172
Device Name: Laparoscope Lens Shield Device
Manufacturer: Medeon Biodesign, Inc.
Device Classification Name: laparoscope, general & plastic surgery
Regulation Number: 876.1500
Classification Product Code: GCJ
Date Received: 01/27/2016
Decision Date: 04/21/2016
Regulation Medical Specialty: Gastroenterology/Urology
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