FDA 510(k), K003322, CODMAN BACTISEAL CATHETERS

FDA 510(k), K003322, CODMAN BACTISEAL CATHETERS

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510(K) Number: K003322
Device Name: CODMAN BACTISEAL CATHETERS
Manufacturer: JAMES M FLAHERTY
Device Classification Name: Catheter, Ventricular
Regulation Number: HCA
Classification Product Code: 10/24/2000
Date Received: 10/01/2001
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Neurology

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