1
/
of
0
FDA 510(k), K060812, POWERPORT(TM)IMPLANTED TITANIUM PORT W/8 FR. CHRONOFLEX CATHETER-MULTIPLE
FDA 510(k), K060812, POWERPORT(TM)IMPLANTED TITANIUM PORT W/8 FR. CHRONOFLEX CATHETER-MULTIPLE
Regular price
$49.00 USD
Regular price
Sale price
$49.00 USD
Unit price
/
per
510(K) Number: K060812
Device Name: POWERPORT(TM)IMPLANTED TITANIUM PORT W/8 FR. CHRONOFLEX CATHETER-MULTIPLE
Manufacturer: C.R. BARD, INC.
Device Classification Name: port & catheter, implanted, subcutaneous, intravascular
Regulation Number: 880.5965
Classification Product Code: LJT
Date Received: 03/24/2006
Decision Date: 07/14/2006
Regulation Medical Specialty: General Hospital
Device Name: POWERPORT(TM)IMPLANTED TITANIUM PORT W/8 FR. CHRONOFLEX CATHETER-MULTIPLE
Manufacturer: C.R. BARD, INC.
Device Classification Name: port & catheter, implanted, subcutaneous, intravascular
Regulation Number: 880.5965
Classification Product Code: LJT
Date Received: 03/24/2006
Decision Date: 07/14/2006
Regulation Medical Specialty: General Hospital
Couldn't load pickup availability
- 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.
View full details