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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