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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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