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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K151396
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MIVI Super 90 Guide Catheters, MIVI Mi-Axus 8F Catheters, REF MIA-9080S (80 cm length); MIA-9090S (9... 2 09/09/2021 FEI # 3011410509
Mivi Neuroscience Inc
MIVI Super 90 8F Guide Catheter, 95 cm, REF MIA-9095S-IDE, For Investigational Use Only; sterile, an... 2 09/09/2021 FEI # 3011410509
Mivi Neuroscience Inc
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