• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Premarket Approval (PMA)

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back to Search Results
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.
 
DeviceENLITE SENSOR
Generic Nameautomated insulin dosing , threshold suspend
Applicant
MEDTRONIC Inc.
18000 devonshire street
northridge, CA 91325-1219
PMA NumberP120010
Supplement NumberS066
Date Received04/20/2015
Decision Date05/15/2015
Product Code OZO 
Advisory Committee Clinical Chemistry
Supplement Type30-day notice
Supplement Reason process change - manufacturer/sterilizer/packager/supplier
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
INCREASE IN THE SHELF LIFE FOR THE ENLITE GLUCOSE SENSORSUBASSEMBLY (SENSOR BASE AND CAPS) AFTER PLASMA TREATMENT, AND AN INCREASE IN THE LOAD (NUMBER)OF TREATED ENLITE SENSOR SUBASSEMBLIES PER PLASMA TREATMENT CYCLE. THE ENLITE GLUCOSE SENSOR IS A COMPONENT OF THE MINIMED 530G SYSTEM.
-
-