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Mivi Neurovascular

FDA Regulatory Profile

Mivi Neurovascular appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 27, 2022.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K213771Merlin Aspiration SystemJanuary 27, 2022
K192558Q3 Distal Access Catheter, Q4 Distal Access Catheter, Q5 Distal Access Catheter, Q6Distal Access CatApril 6, 2020

FDA data resources