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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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