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FDA 510(k), K833417, ENDOSCOPIC RETROGRADE
FDA 510(k), K833417, ENDOSCOPIC RETROGRADE
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$49.00 USD
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$49.00 USD
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510(K) Number: K833417
Device Name: ENDOSCOPIC RETROGRADE
Manufacturer:
Device Classification Name: Endoscopic Retrograde Cholangiopancreatography (Ercp) Cannula
Regulation Number: ODD
Classification Product Code: KXA
Date Received: 10/03/1983
Decision Date: 11/28/1983
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: ENDOSCOPIC RETROGRADE
Manufacturer:
Device Classification Name: Endoscopic Retrograde Cholangiopancreatography (Ercp) Cannula
Regulation Number: ODD
Classification Product Code: KXA
Date Received: 10/03/1983
Decision Date: 11/28/1983
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Gastroenterology/Urology
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