• 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
 

 
 
7 records meeting your search criteria returned- Product Code: LRC Patient Problem: Hemorrhage/Bleeding Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
WILLIAM COOK EUROPE FROVA INTUBATING INTRODUCER 02/14/2017
ACCLARENT, INC. RELIEVA SPIN SINUPLASTY SYSTEM 04/11/2016
ACCLARENT, INC. RELIEVA SPIN SINUPLASTY SYSTEM 11/09/2015
ACCLARENT RELIEVA SPIN SINUPLASTY SYSTEM 05/04/2015
ACCLARENT RELIEVA SPIN SINUPLASTY SYSTEM 04/30/2015
ACCLARENT, INC. RELIEVA SPIN BALLOON SINUPLASTY SYSTEM 09/26/2014
ACCLARENT RELIEVA SPIN BALLOON SINUPLASTY SYSTEM 09/10/2014
-
-