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

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 
 
 
11 records meeting your search criteria returned- Product Code: OCL Product Problem: Device Dislodged or Dislocated Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ATRICURE, INC. SUBTLE CANNULA WITH GUIDE 12/21/2018
ATRICURE, INC. COBRA FUSION 150 ABLATION MINIMALLY INVA 08/03/2017
ATRICURE, INC. COBRA FUSION 150 ABLATION MINIMALLY INVA 07/26/2017
ATRICURE, INC. COBRA FUSION MAGNETIC RETRIEVER SYSTEM 06/20/2017
ATRICURE, INC. COBRA FUSION 150 ABLATION SYSTEM 08/10/2016
ATRICURE INC. COBRA FUSION 150 ABLATION SYSTEM 10/02/2015
ATRICURE, INC. COBRA FUSION MAGNETIC RETRIEVER SYSTEM 08/31/2015
ATRICURE, INC. COBRA FUSION 150 MINIMALLY INVASIVE ABLA 08/12/2015
ATRICURE, INC. COBRA FUSION MAGNETIC RETRIEVER SYSTEM 08/12/2015
ATRICURE, INC. COBRA FUSION 150 SURGICAL SYSTEM 08/04/2015
-
-