Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience
  • Print
  • Share
  • E-mail
-
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
 

 
 
 1 
 2 
 > 
 
19 records meeting your search criteria returned- Product Code: OOI Patient Problem: No Known Impact Or Consequence To Patient Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ABBOTT MOLECULAR, INC. ALINITY M SYSTEM 08/21/2020
BECTON, DICKINSON & CO. BD INSTRUMENT MAX CLINICAL 07/29/2020
ABBOTT MOLECULAR, INC. ALINITY M SYSTEM 07/22/2020
BECTON, DICKINSON & CO. BD INSTRUMENT MAX CLINICAL 07/17/2020
BECTON, DICKINSON & CO. INSTRUMENT MAX CLINICAL 07/15/2020
BECTON, DICKINSON & CO. INSTRUMENT MAX CLINICAL 07/15/2020
ABBOTT MOLECULAR, INC. ALINITY M SYSTEM 07/14/2020
ABBOTT MOLECULAR, INC. ALINITY M SYSTEM 06/29/2020
ABBOTT MOLECULAR, INC. ALINITY M SYSTEM 06/29/2020
BECTON, DICKINSON & CO. INSTRUMENT MAX CLINICAL 06/17/2020
-
-