FDA 510(k), K120766, ENDOSCOPIC DIAGNOSTIC & TREATMENT SYSTEM (MODIFICATION)

FDA 510(k), K120766, ENDOSCOPIC DIAGNOSTIC & TREATMENT SYSTEM (MODIFICATION)

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510(K) Number: K120766
Device Name: ENDOSCOPIC DIAGNOSTIC & TREATMENT SYSTEM (MODIFICATION)
Manufacturer:
Device Classification Name: Cystoscope And Accessories, Flexible/Rigid
Regulation Number: 876.1500
Classification Product Code: FAJ
Date Received: 03/13/2012
Decision Date: 09/11/2012
Regulation Medical Specialty: Gastroenterology/Urology
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