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FDA 510(k) Applications Submitted by ANIARA DIAGNOSTICA ,LLC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K083729
12/16/2008
HEMOCLOT QUANTI- V-L, FACTOR V-L CALIBRATOR, BIOPHEN V-L CAL (UNDILUTED), BIOPHEN ACT. PC-R CONTROL PLASMA AND BIOPHEN
ANIARA DIAGNOSTICA ,LLC
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