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FDA 510(k) Applications Submitted by BABU PERIASAMY
FDA 510(k) Number
Submission Date
Device Name
Applicant
K171808
06/19/2017
TDM Plate and Screw System
TDM Co. Ltd.
K123532
11/16/2012
OCELOT PIXL CATHETER
AVINGER, INC.
K143412
11/28/2014
ADROIT Guiding Catheter
CORDIS CORPORATION
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