FDA 510(k), K131131, E.G. SCAN(TM) II ESOPHAGOSCOPE SYSTEM

FDA 510(k), K131131, E.G. SCAN(TM) II ESOPHAGOSCOPE SYSTEM

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510(K) Number: K131131
Device Name: E.G. SCAN(TM) II ESOPHAGOSCOPE SYSTEM
Manufacturer:
Device Classification Name: Esophagoscope (Flexible Or Rigid)
Regulation Number: 874.4710
Classification Product Code: EOX
Date Received: 04/22/2013
Decision Date: 06/21/2013
Regulation Medical Specialty: Ear Nose & Throat
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