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FDA 510(k) Applications Submitted by ALEX FERRI
FDA 510(k) Number
Submission Date
Device Name
Applicant
K133685
12/02/2013
0.9% SODIUM CHLORIDE FLUSH SYRINGE
AMUSA
K241312
05/09/2024
TeraRecon Cardiac.Chambers.MR (1.0.0)
TeraRecon,Inc.
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