FDA 510(k), K123223, EC SINGLE USE, POLYPECTOMY SNARE

FDA 510(k), K123223, EC SINGLE USE, POLYPECTOMY SNARE

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510(K) Number: K123223
Device Name: EC SINGLE USE, POLYPECTOMY SNARE
Manufacturer:
Device Classification Name: Snare, Flexible
Regulation Number: 876.4300
Classification Product Code: FDI
Date Received: 10/15/2012
Decision Date: 01/10/2013
Regulation Medical Specialty: Gastroenterology/Urology
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