FDA 510(k) Applications Submitted by MICHAEL ACOSTA

FDA 510(k) Number Submission Date Device Name Applicant
K091021 04/09/2009 MODIFICATION TO MEDICOMPASS CONNECT IMETRIKUS, INC.
K212779 09/01/2021 Coag-Sense Prothrombin (PT) / INR Monitoring System for Patient Self-Testing CoaguSense, Inc.


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