FDA 510(k) Applications Submitted by NANO-DITECH CORPORATION

FDA 510(k) Number Submission Date Device Name Applicant
K102131 07/29/2010 NANO-CHECK AMI CTNI CARDIAC MARKER TEST NANO-DITECH CORPORATION
K102441 07/29/2010 NANO-CHECK AMI 2 IN 1 CARDIAC MARKER, CTNL AND MYOGLOBIN NANO-DITECH CORPORATION


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