• 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 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
221 records meeting your search criteria returned- Product Code: FAJ Product Problem: Microbial Contamination of Device Report Date From: 01/1/2016
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
OLYMPUS MEDICAL SYSTEMS CORP. OES CYSTONEPHROFIBERSCOPE 10/21/2021
OLYMPUS MEDICAL SYSTEMS CORP. CYSTO-NEPHRO VIDEOSCOPE 10/13/2021
OLYMPUS MEDICAL SYSTEMS CORP. OES CYSTONEPHROFIBERSCOPE 10/12/2021
OLYMPUS MEDICAL SYSTEMS CORP. OES CYSTONEPHROFIBERSCOPE 10/08/2021
OLYMPUS MEDICAL SYSTEMS CORP. FIBERSCOPE "CYF-5A", WITH SUCTION, EUROP 09/28/2021
OLYMPUS MEDICAL SYSTEMS CORP. OES CYSTONEPHROFIBERSCOPE 09/14/2021
OLYMPUS MEDICAL SYSTEMS CORP. OES CYSTONEPHROFIBERSCOPE 09/09/2021
OLYMPUS MEDICAL SYSTEMS CORP. OES CYSTONEPHROFIBERSCOPE 08/31/2021
OLYMPUS MEDICAL SYSTEMS CORP. OES CYSTONEPHROFIBERSCOPE 08/30/2021
OLYMPUS MEDICAL SYSTEMS CORP. OES CYSTONEPHROFIBERSCOPE 08/27/2021
-
-