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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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500 records meeting your search criteria returned. The results are incomplete - please narrow your search.
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ManufacturerBrand NameDate Report Received
MICRO THERAPEUTICS, INC. DBA EV3 SOLITAIRE FR 07/11/2022
IMPERATIVE CARE. INC ZOOM REPERFUSION CATHETER 07/05/2022
PENUMBRA, INC. PENUMBRA SYSTEM ACE 68 REPERFUSION CATHE 06/30/2022
PENUMBRA, INC. PENUMBRA SYSTEM JET7 REPERFUSION CATHETE 06/24/2022
PENUMBRA, INC. PENUMBRA SYSTEM ACE 68 REPERFUSION CATHE 06/24/2022
PENUMBRA, INC. PENUMBRA SYSTEM 3MAX REPERFUSION CATHETE 06/21/2022
MICRO THERAPEUTICS, INC. DBA EV3 SOLITAIRE FR 06/20/2022
MICRO THERAPEUTICS, INC. DBA EV3 SOLITAIRE FR4 06/16/2022
MICRO THERAPEUTICS, INC. DBA EV3 SOLITAIRE FR 06/15/2022
PENUMBRA, INC. PENUMBRA SYSTEM RED62 REPERFUSION CATHET 06/14/2022
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