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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.
 
Trade NameBLU-U
Classification Namesystem, laser, photodynamic therapy
Generic Nameblue light photodynamic therapy illuminator
ApplicantDUSA PHARMACEUTICALS, INC.
PMA NumberP990019
Supplement NumberS002
Date Received09/30/2002
Decision Date01/09/2003
Product Code
MVF[ Registered Establishments with MVF ]
Advisory Committee General & Plastic Surgery
Supplement Typenormal 180 day track
Supplement Reason change design/components/specifications - specifications
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for extension of the calibration interval from the currently approved 500 cycles (with a 50 cycle buffer) to 1600 cycles (with a 50 cycle buffer).
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