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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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9 records meeting your search criteria returned- Product Code: DQO Product Problem: Defective Device Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
LIGHTLAB IMAGING, INC. DRAGONFLY 07/15/2022
BOSTON SCIENTIFIC CORPORATION FLOSWITCH HP 10/28/2020
MEDTRONIC, INC DXTERITY TRA 03/04/2020
MICROVENTION INC. SOFIA 5F-125CM STR 01/07/2020
BOSTON SCIENTIFIC CORPORATION FLOSWITCH HP 10/01/2019
EDWARDS LIFESCIENCES LLC SWAN-GANZ 06/05/2019
CORDIS CASHEL 466P306X 12/27/2018
DEROYAL INDUSTRIES, INC. THERMODILUTION CATHETER, 7FR 4 LUMEN 09/28/2017
ANGIODYNAMICS, INC. ACCUVU 08/23/2017
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