FDA 510(k), K093624, OPTISCAN MODEL OPTISCAN CEIS
FDA 510(k), K093624, OPTISCAN MODEL OPTISCAN CEIS
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510(K) Number: K093624
Device Name: OPTISCAN MODEL OPTISCAN CEIS
Manufacturer:
Device Classification Name: Laparoscope, General & Plastic Surgery
Regulation Number: 876.1500
Classification Product Code: GCJ
Date Received: 11/23/2009
Decision Date: 03/05/2010
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: OPTISCAN MODEL OPTISCAN CEIS
Manufacturer:
Device Classification Name: Laparoscope, General & Plastic Surgery
Regulation Number: 876.1500
Classification Product Code: GCJ
Date Received: 11/23/2009
Decision Date: 03/05/2010
Regulation Medical Specialty: Gastroenterology/Urology