• 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 
 > 
 
58 records meeting your search criteria returned- Product Code: FFT Patient Problem: Insufficient Information Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
GIVEN IMAGING LTD., YOQNEAM BRAVO 09/19/2023
GIVEN IMAGING LTD. BRAVO PH MONITORING SYSTEM 08/12/2023
GIVEN IMAGING LTD., YOQNEAM BRAVO 04/17/2023
GIVEN IMAGING LTD., YOQNEAM BRAVO 10/07/2022
GIVEN IMAGING LTD., YOQNEAM BRAVO 10/06/2022
GIVEN IMAGING LTD., YOQNEAM BRAVO 10/04/2022
GIVEN IMAGING LTD., YOQNEAM BRAVO 09/28/2022
MEDTRONIC/GIVEN IMAGING INC. BRAVO CAPSULE 08/15/2022
COVIDIEN LLC / GIVEN IMAGING LTD. BRAVO CF CAPSULE 05/13/2022
MEDTRONICS GIVEN IMAGING LTD. MEDTRONICS BRAVO CF RECORDER 03/02/2022
-
-