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 
 3 
 4 
 > 
 
31 records meeting your search criteria returned- Product Code: FPA Patient Problem: Bradycardia Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CAREFUSION ALARIS PUMP MODULE ADMINISTRATION SET 07/22/2019
CAREFUSION ALARIS SYRINGE ADAPTER SET 06/03/2019
CAREFUSION ALARIS PUMP MODULE 04/09/2019
CAREFUSION MICROBORE EXTENSION SET 02/08/2019
CAREFUSION 303, INC. MICROBORE TUBING EXTENSION SET 01/11/2019
CAREFUSION ALARIS® PUMP MODULE ADMINISTRATION SET 11/09/2018
CAREFUSION MICROBORE EXTENSION SET 03/09/2018
CAREFUSION 6-IN STANDARDBORE EXTENSION SET 08/25/2017
CAREFUSION 303, INC. MAXGUARD 07/31/2017
BAXTER HEALTHCARE - AIBONITO ONE-LINK NEUTRAL LUER ACTIVATED DEVICE 06/26/2017
-
-