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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
 

 
 
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15 records meeting your search criteria returned- Product Code: DRG Product Problem: No Display/Image Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
NIHON KOHDEN CORPORATION ORG-9110A 04/27/2023
NIHON KOHDEN CORPORATION ORG-9110A 04/20/2023
NKUS LAB CENTRAL MONITORING SYSTEM 02/21/2020
NKUS LAB CENTRAL MONITORING SYSTEM 01/16/2019
NKUS LAB CENTRAL MONITORING SYSTEM 02/16/2018
NKUS LAB CENTRAL MONITORING SYSTEM 11/08/2017
NIHON KOHDEN CORPORATION ORG-9110A 07/14/2017
NIHON KOHDEN CORPORATION ORG-9110A 07/14/2017
NKUS LAB CENTRAL MONITORING SYSTEM 06/27/2017
NKUS LAB CENTRAL MONITORING SYSTEM 01/27/2017
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