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 
 > 
 
15 records meeting your search criteria returned- Product Code: DQA Product Problem: Inappropriate/Inadequate Shock/Stimulation Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MASIMO - 40 PARKER LNCS DC-I 01/25/2019
MASIMO - 40 PARKER RADICAL, HANDHELD 02/04/2018
MASIMO - 40 PARKER RD SET NEO 03/31/2017
GE MEDICAL SYSTEMS INFORMATION TECHNOLOG CARESCAPE V100 03/20/2017
MASIMO - 40 PARKER RADIUS-7 02/14/2017
MASIMO - 40 PARKER RD SET NEO 02/10/2017
MASIMO - 40 PARKER RADICAL-7 10/21/2016
COVIDIEN NELLCOR 06/24/2016
MASIMO CORPORATION RADICAL-7 05/27/2016
MASIMO CORPORATION LNCS ADTX ADHESIVE SENSOR 05/29/2015
-
-