• 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 
 3 
 4 
 5 
 
 
50 records meeting your search criteria returned- Product Code: LPB Patient Problem: Ventricular Fibrillation Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOSENSE WEBSTER INC THERMOCOOL SF BI-DIRECTIONAL CATHETER 07/08/2020
BIOSENSE WEBSTER INC THERMOCOOL® SMART TOUCH® SF BI-DIRECTION 11/14/2019
BIOSENSE WEBSTER INC THERMOCOOL® SMART TOUCH® SF UNI-DIRECTIO 09/18/2019
BIOSENSE WEBSTER INC. THERMOCOOL® SMART TOUCH® SF BI-DIRECTION 08/29/2019
BIOSENSE WEBSTER INC. THERMOCOOL® SMART TOUCH® SF BI-DIRECTION 06/05/2019
BIOSENSE WEBSTER INC. THERMOCOOL® SMART TOUCH® SF BI-DIRECTION 05/10/2019
BIOSENSE WEBSTER INC THERMOCOOL® SMART TOUCH¿ ELECTROPHYSIOLO 03/29/2019
BIOSENSE WEBSTER INC. EZ STEER¿ NAV BI-DIRECTIONAL ELECTROPHYS 03/15/2019
BIOSENSE WEBSTER INC. UNK_SMART TOUCH BIDIRECTIONAL SF 02/19/2019
BIOSENSE WEBSTER INC THMCL SMTCH SF BID, TC, D-F 01/04/2019
-
-