FDA 510(k), K151604, 23ga Chandelier Illuminator, 25ga Chandelier Illuminator

FDA 510(k), K151604, 23ga Chandelier Illuminator, 25ga Chandelier Illuminator

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510(K) Number: K151604
Device Name: 23ga Chandelier Illuminator, 25ga Chandelier Illuminator
Manufacturer: PEREGRINE SURGICAL LTD.
Device Classification Name: endoilluminator
Regulation Number: 876.1500
Classification Product Code: MPA
Date Received: 06/15/2015
Decision Date: 09/11/2015
Regulation Medical Specialty: Gastroenterology/Urology

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