FDA 510(k), K140763, MONOFILAMENT POLYPECTOMY SNARE

FDA 510(k), K140763, MONOFILAMENT POLYPECTOMY SNARE

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510(K) Number: K140763
Device Name: MONOFILAMENT POLYPECTOMY SNARE
Manufacturer:
Device Classification Name: Snare, Flexible
Regulation Number: 876.4300
Classification Product Code: FDI
Date Received: 03/27/2014
Decision Date: 04/24/2014
Regulation Medical Specialty: Gastroenterology/Urology
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