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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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6 records meeting your search criteria returned- Product Code: JAQ Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
MERIT MEDICAL SYSTEMS SAVI 03/31/2021
NUCLETRON B.V. PROGUIDE SHARP NEEDLE 12/23/2020
HOLOGIC, INC. CONTURA MLB CATHETER WITH TRICONCAVE 10/18/2017
NUCLETRON FLEXITRON 02/11/2016
VARIAN MEDICAL SYSTEMS, INC. GAMMAMED 05/28/2014
VARIAN MEDICAL SYSTEMS, INC. FLETCHER-SUIT-DELCOS-STYLE APPLICATOR SE 01/31/2014
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