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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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