FDA 510(k), K001217, INSIDE VIEW
FDA 510(k), K001217, INSIDE VIEW
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$149.00 USD
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510(K) Number: K001217
Device Name: INSIDE VIEW
Manufacturer:
Device Classification Name: Endoscope, Rigid
Regulation Number: 876.1500
Classification Product Code: GCM
Date Received: 04/17/2000
Decision Date: 07/11/2000
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: INSIDE VIEW
Manufacturer:
Device Classification Name: Endoscope, Rigid
Regulation Number: 876.1500
Classification Product Code: GCM
Date Received: 04/17/2000
Decision Date: 07/11/2000
Regulation Medical Specialty: Gastroenterology/Urology