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FDA 510(k), K910769, SURGITEK(R) ERCP CONTRAST MEDIA SYSTEM
FDA 510(k), K910769, SURGITEK(R) ERCP CONTRAST MEDIA SYSTEM
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$149.00 USD
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$149.00 USD
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510(K) Number: K910769
Device Name: SURGITEK(R) ERCP CONTRAST MEDIA SYSTEM
Manufacturer:
Device Classification Name: Endoscopic Retrograde Cholangiopancreatography (Ercp) Cannula
Regulation Number: 876.1500
Classification Product Code: ODD
Date Received: 02/22/1991
Decision Date: 06/25/1991
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: SURGITEK(R) ERCP CONTRAST MEDIA SYSTEM
Manufacturer:
Device Classification Name: Endoscopic Retrograde Cholangiopancreatography (Ercp) Cannula
Regulation Number: 876.1500
Classification Product Code: ODD
Date Received: 02/22/1991
Decision Date: 06/25/1991
Regulation Medical Specialty: Gastroenterology/Urology
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