• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

  • 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 
 > 
 
16 records meeting your search criteria returned- Product Code: FDX Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BOSTON SCIENTIFIC CORPORATION RX CYTOLOGY BRUSH 03/12/2024
BOSTON SCIENTIFIC CORPORATION RX CYTOLOGY BRUSH 12/14/2023
HOBBS MEDICAL, INC. SUPERDIMENSION CYTOLOGY BRUSH 08/28/2023
COVIDIEN LP - SUPERDIMENSION INC UNKNOWN CYTOLOGY BRUSH 08/09/2023
BOSTON SCIENTIFIC CORPORATION RX CYTOLOGY BRUSH 04/12/2023
AOMORI OLYMPUS CO., LTD. SINGLE USE CYTOLOGY BRUSH V 04/05/2023
HOBBS MEDICAL, INC. UNKOWN CYTOLOGY BRUSH 03/22/2023
BOSTON SCIENTIFIC CORPORATION RX CYTOLOGY BRUSH 03/09/2023
COVIDIEN LP - SUPERDIMENSION INC UNKNOWN CYTOLOGY BRUSH 03/07/2023
BOSTON SCIENTIFIC CORPORATION RX CYTOLOGY BRUSH 10/12/2022
-
-