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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
 

 
 
7 records meeting your search criteria returned- Product Code: DRG Product Problem: Incorrect, Inadequate or Imprecise Resultor Readings Report Date From: 01/1/2016
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ManufacturerBrand NameDate Report Received
NIHON KOHDEN CORPORATION ORG-9110A 04/20/2021
NIHON KOHDEN CORPORATION ORG-9110A 04/19/2021
NKUS LAB CENTRAL MONITORING SYSTEM 02/05/2021
NIHON KOHDEN CORPORATION ORG-9110A 07/21/2020
NIHON KOHDEN CORPORATION ZM-930PA 07/16/2020
NIHON KOHDEN CORPORATION ORG-9110A 08/08/2018
IDEAL LIFE IDEAL LIFE BLOOD PRESSURE MONITOR 07/26/2016
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