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U.S. Department of Health and Human Services

Premarket Approval (PMA)

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Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
Classification Namelipoprotein, low density, removal
Generic Namelipoprotein, low density, removal
546 fifth ave., 21st floor
new york, NY 10036
PMA NumberP910018
Supplement NumberS016
Date Received05/21/2012
Decision Date06/19/2012
Product Code
MMY[ Registered Establishments with MMY ]
Advisory Committee Gastroenterology/Urology
Supplement Type30-day notice
Supplement Reason process change - manufacturer/sterilizer/packager/supplier
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Change in the location of a supplier¿s manufacturing facility that produces components used in the manufacturing of the device.