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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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