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U.S. Department of Health and Human Services

Devices@FDA
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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.
 
DeviceFreeStyle Libre Pro Flash Glucose Monitoring System
Generic NameSensor, glucose, invasive
ApplicantAbbott Diabetes Care, Inc.
1360 S. Loop Rd.
Alameda, CA 94502
PMA NumberP150021
Supplement NumberS023
Date Received03/05/2018
Decision Date04/05/2018
Product Code MDS 
Advisory Committee Clinical Chemistry
Clinical TrialsNCT02073058
Supplement Type30-Day Notice
Supplement Reason Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
Change to increase the sensor manufacturing capacity, at the manufacturing facility ADC Witney, by implementing a high volume sensor manufacturing line setup. The change included qualification of a new ISO 8 cleanroom and implementation of new manufacturing and support equipment. The sensor is a component of the Freestyle Libre Flash Pro and FreeStyle Libre Flash Glucose Monitoring System.
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