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

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 
 > 
 
45 records meeting your search criteria returned- Product Code: OCL Patient Problem: Death Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ATRICURE, INC. NUMERIS TETHERED COAGULATION SYSTEM WITH 11/13/2018
ATRICURE, INC. COOLRAIL LINEAR PEN 08/21/2018
ATRICURE, INC. EPI-SENSE GUIDED COAGULATION SYSTEM WITH 08/14/2018
ATRICURE, INC. COBRA FUSION 150 ABLATION SYSTEM 07/03/2018
ATRICURE, INC. EPI-SENSE GUIDED COAGULATION SYSTEM WITH 07/02/2018
ATRICURE, INC. EPI-SENSE GUIDED COAGULATION SYSTEM WITH 06/29/2018
ATRICURE, INC. EPI-SENSE GUIDED COAGULATION SYSTEM WITH 03/14/2018
ATRICURE, INC. EPI-SENSE GUIDED COAGULATION SYSTEM WITH 01/04/2018
ATRICURE, INC. ATRICURE BIPOLAR SYSTEM 01/04/2018
ATRICURE, INC. EPI-SENSE GUIDED COAGULATION SYSTEM WITH 12/12/2017
-
-