Note: This medical device record is a PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information. |
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Device | VASCULAR SOLUTIONS DUETT SEALING DEVICE |
Generic Name | Device, hemostasis, vascular |
Applicant | Vascular Solutions, Inc. 6464 SYCAMORE COURT NORTH MINNEAPOLIS, MN 55369 |
PMA Number | P990037 |
Supplement Number | S009 |
Date Received | 03/15/2002 |
Decision Date | 04/03/2002 |
Product Code |
MGB |
Advisory Committee |
Cardiovascular |
Supplement Type | Real-Time Process |
Supplement Reason | Change Design/Components/Specifications/Material |
Expedited Review Granted? | No |
Combination Product | No |
Recalls | CDRH Recalls |
Approval Order Statement APPROVAL FOR A DESIGN CHANGE TO THE DUETT SEALING DEVICE AND DIAGNOSTIC DUETT SEALING DEVICE. SPECIFICALLY, A RELIEF VALVE COMPONENT WILL REPLACE THE PILOT BALLOON ASSEMBLY ON BOTH DEVICES. |
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