FDA 510(k) Applications Submitted by BODITECH MED INC.

FDA 510(k) Number Submission Date Device Name Applicant
K170232 01/25/2017 AFIAS TSH-SP, AFIAS TSH-VB, AFIAS-6/SP Analyzer, AFIAS-6/VB Analyzer BODITECH MED INC.
K132167 07/12/2013 I-CHROMA IFOB WITH I-CHROMA READER Boditech Med Inc.


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