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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 
4 records meeting your search criteria returned- Product Code: JAK Product Problem: Inadequate or Insufficient Training Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
NEUROLOGICA CORPORATION OMNITOM 11/19/2021
NEUROLOGICA CORPORATION OMNITOM 07/31/2021
SIEMENS HEALTHCARE GMBH SOMATOM GO.ALL 05/25/2021
SIEMENS HEALTHCARE GMBH SOMATOM GO.UP 05/21/2021
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