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FDA 510(k) Applications for Medical Device Product Code "LXG"
(Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use)
FDA 510(k) Number
Applicant
Device Name
Decision Date
K021927
BIOMET, INC.
PLATELET CONCENTRATE SEPARATION KIT FOR CELSEP CENTRIFUGE SYSTEM
07/12/2002
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