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FDA 510(k) Applications Submitted by NANOGEN, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K083430
11/19/2008
REAL-TIME PCR INTERNAL CONTROL 2B SET
NANOGEN, INC.
K051596
06/16/2005
STATUSFIRST CHF (CONGESTIVE HEART FAILURE) NT-PROBNP, MODEL 20204
NANOGEN, INC.
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