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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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16 records meeting your search criteria returned- Product Code: JAK Product Problem: No Apparent Adverse Event Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
GE HANGWEI MEDICAL SYSTEMS CO., LTD. CT 750HD 12/22/2021
SIEMENS HEALTHCARE GMBH SOMATOM FORCE 11/29/2021
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. IQON SPECTRAL CT 11/10/2021
GE MEDICAL SYSTEMS, LLC REVOLUTION CT 07/30/2021
GE HEALTHCARE JAPAN CORPORATION BRIGHTSPEED CT 05/16/2014
GE HANGWEI MEDICAL SYSTEMS CO., LTD. BRIGHTSPEED CT 04/11/2014
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