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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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176 records meeting your search criteria returned- Product Code: DRT Patient Problem: No Consequences Or Impact To Patient Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
WELCH ALLYN INC. 242CS/POLISH/SPN/WAFN/PLUGC 10/26/2020
NIHON KOHDEN CORPORATION ZM-531PA 08/28/2020
NIHON KOHDEN CORPORATION GZ-120PA 08/27/2020
NIHON KOHDEN CORPORATION ZM-531PA 08/22/2020
NIHON KOHDEN CORPORATION GZ-120PA 08/20/2020
NIHON KOHDEN CORPORATION GZ-140PA 08/04/2020
NIHON KOHDEN CORPORATION ZM-530PA 07/21/2020
NIHON KOHDEN CORPORATION ZM-520PA 07/07/2020
NIHON KOHDEN CORPORATION GZ-120PA 06/04/2020
NIHON KOHDEN CORPORATION GZ-120PA 06/04/2020
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