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 | SYNCHROMED II INFUSION SYSTEM |
Applicant | MEDTRONIC Inc. 7000 CENTRAL AVENUE NE MINNEAPOLIS, MN 55432-3576 |
PMA Number | P860004 |
Supplement Number | S112 |
Date Received | 08/21/2009 |
Decision Date | 09/18/2009 |
Advisory Committee |
General Hospital |
Supplement Type | 30-Day Notice |
Supplement Reason | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
Expedited Review Granted? | No |
Combination Product | No |
Approval Order Statement AUTOMATION OF THE TRANSFER OF FINAL FUNCTIONAL TEST DATA TO FACTORYWORKS, THE MANUFACTURING SOFTWARE THAT CONTROLS THE MANUFACTURING OF THE DEVICE. |
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