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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
PENUMBRA, INC. RED 72 03/25/2022
PENUMBRA, INC. PENUMBRA SYSTEM RED 72 REPERFUSION CATHE 03/21/2022
MICRO THERAPEUTICS, INC. DBA EV3 SOLITAIRE FR 03/18/2022
IMPERATIVE CARE. INC ZOOM REPERFUSION CATHETER 03/16/2022
IMPERATIVE CARE. INC ZOOM REPERFUSION CATHETER 03/16/2022
PENUMBRA, INC. PENUMBRA SYSTEM 3MAX REPERFUSION CATHETE 03/12/2022
PENUMBRA, INC. PENUMBRA SYSTEM RED72 REPERFUSION CATHET 03/11/2022
MICRO THERAPEUTICS, INC. DBA EV3 SOLITAIRE FR 03/11/2022
IMPERATIVE CARE. INC ZOOM REPERFUSION CATHETER 03/04/2022
PENUMBRA, INC. PENUMBRA SYSTEM RED72 REPERFUSION CATHET 03/01/2022
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