• 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 
 > 
 
13 records meeting your search criteria returned- Product Code: MNO Patient Problem: No Known Impact Or Consequence To Patient Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CRYOLIFE, INC. SOLOGRIP III HANDPIECE 06/02/2017
CRYOLIFE, INC. SOLOGRIP III HANDPIECE 01/22/2016
CRYOLIFE, INC. SOLARGEN 2100S CONSOLE 06/09/2015
CRYOLIFE, INC. SOLARGEN 2100S CONSOLE 04/13/2015
CRYOLIFE, INC. TMR 2000 TRANSMYOCARDIAL REVASCULARIZATI 03/27/2015
CARDIOGENESIS CORPORATION SOLARGEN 2100S TRANSYMOCARDIAL REVASCULA 12/22/2014
CARDIOGENESIS CORPORATION TMR 2000 TRANSMYOCARDIAL REVASCULARIZATI 12/22/2014
CARDIOGENESIS CORPORATION SOLARGEN 2100S TRANSMYOCARDIAL REVASCULA 10/03/2014
CARDIOGENESIS CORPORATION PEARL 5.0 HANDPIECE 09/22/2014
CARDIOGENESIS CORPORATION PEARL 5.0 HANDPIECE 09/22/2014
-
-