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
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
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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