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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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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
 

 
 
3 records meeting your search criteria returned- Product Code: KQO Patient Problem: Insufficient Information Report Date From: 01/1/2019

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ManufacturerBrand NameDate Report Received
BECKMAN COULTER IQ 200 URINE ANALYZER BODY FLUIDS MODULE 10/26/2023
SIEMENS HEALTHCARE DIAGNOSTICS CLINITEK ATLAS 03/08/2021
ROCHE DIAGNOSTICS URISYS 1100 10/28/2020
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