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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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3 records meeting your search criteria returned- Product Code: JAK Product Problem: Device Fell Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
NEUSOFT MEDICAL SYSTEMS CO., LTD. NEUVIZ 64 IN 10/29/2019
NEUSOFT MEDICAL SYSTEMS CO., LTD. CT SCAN 10/07/2019
BAYER MEDICAL CARE, INC. OVERHEAD COUNTERPOISE SYSTEM 07/26/2018
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