FDA 510(k), K150781, Tissue Removal Pouch

FDA 510(k), K150781, Tissue Removal Pouch

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510(K) Number: K150781
Device Name: Tissue Removal Pouch
Manufacturer: BOEHRINGER LABORATORIES, LLC
Device Classification Name: Laparoscope, General & Plastic Surgery
Regulation Number: 876.1500
Classification Product Code: GCJ
Date Received: 03/25/2015
Decision Date: 06/19/2015
Regulation Medical Specialty: Gastroenterology/Urology

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