FDA 510(k) Applications Submitted by Janel Hurtado

FDA 510(k) Number Submission Date Device Name Applicant
K212402 08/02/2021 MIVI Q Distal Access Catheter MIVI Neuroscience, Inc.
K192558 09/17/2019 Q3 Distal Access Catheter, Q4 Distal Access Catheter, Q5 Distal Access Catheter, Q6Distal Access Catheter MIVI Neurovascular
K213771 12/02/2021 Merlin Aspiration System MIVI Neurovascular, Inc.


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