FDA 510(k), K131991, ENDOCHOICE HOT BIOPSY FORCEPS

FDA 510(k), K131991, ENDOCHOICE HOT BIOPSY FORCEPS

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510(K) Number: K131991
Device Name: ENDOCHOICE HOT BIOPSY FORCEPS
Manufacturer:
Device Classification Name: Forceps, Biopsy, Electric
Regulation Number: 876.4300
Classification Product Code: KGE
Date Received: 06/28/2013
Decision Date: 10/15/2013
Regulation Medical Specialty: Gastroenterology/Urology
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