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FDA 510(k), K090512, POWERPORT DUO M.R.I. IMPLANTED PORT WITH 9.5 FR. DUAL LUMEN CHRONOFLEX POLYURETHANE CATHETER
FDA 510(k), K090512, POWERPORT DUO M.R.I. IMPLANTED PORT WITH 9.5 FR. DUAL LUMEN CHRONOFLEX POLYURETHANE CATHETER
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510(K) Number: K090512
Device Name: POWERPORT DUO M.R.I. IMPLANTED PORT WITH 9.5 FR. DUAL LUMEN CHRONOFLEX POLYURETHANE CATHETER
Manufacturer: C.R. BARD, INC.
Device Classification Name: port & catheter, implanted, subcutaneous, intravascular
Regulation Number: 880.5965
Classification Product Code: LJT
Date Received: 02/26/2009
Decision Date: 03/27/2009
Regulation Medical Specialty: General Hospital
Device Name: POWERPORT DUO M.R.I. IMPLANTED PORT WITH 9.5 FR. DUAL LUMEN CHRONOFLEX POLYURETHANE CATHETER
Manufacturer: C.R. BARD, INC.
Device Classification Name: port & catheter, implanted, subcutaneous, intravascular
Regulation Number: 880.5965
Classification Product Code: LJT
Date Received: 02/26/2009
Decision Date: 03/27/2009
Regulation Medical Specialty: General Hospital
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- 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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