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 | MYSENTRY SYSTEM ; MYSENTRY MONITOR |
Generic Name | Sensor, glucose, invasive |
Applicant | MEDTRONIC MINIMED 18000 DEVONSHIRE ST NORTHRIDGE, CA 91325 |
PMA Number | P980022 |
Supplement Number | S169 |
Date Received | 10/31/2014 |
Decision Date | 11/26/2014 |
Product Codes |
MDS OYC |
Advisory Committee |
Clinical Chemistry |
Supplement Type | 30-Day Notice |
Supplement Reason | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
Expedited Review Granted? | No |
Combination Product | No |
Approval Order Statement CHANGE TO THE MOLD USED IN THE MANUFACTURING OF THE USB CONNECTOR, A COMPONENT IN THE MYSENTRY MONITOR THAT IS USED TO RECEIVE DATA FROM THE PARADIGM REAL-TIME REVEL SYSTEM. |
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