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
 

 
 
8 records meeting your search criteria returned- Product Code: HIB Product Problem: Shipping Damage or Problem Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
WELCH ALLYN, INC. KLEENSPEC 590 SEERIES DISP. VIGINAL SPEC 02/11/2015
WELCH ALLYN, INC. KLEENSPEC 590 SERIES DISP. VAGINAL SPECU 01/28/2015
WELCH ALLYN, INC. KLEENSPEC 590 SERIES DISP. VAGINAL SPECU 01/13/2015
WELCH ALLYN KLEENSPEC590 SERIES DISP. VAGINAL SPECUL 12/17/2014
WELCH ALLYN, INC. KLEENSPEC 590 SERIES DISP. VAGINAL SPECU 11/05/2014
WELCH ALLYN, INC. KLEENSPEC 590 SERIES DISP. VAGINAL SPECU 10/29/2014
WELCH ALLYN KLEENSPEC 590 SERIES DISP. VAGINAL SPECU 10/01/2014
WELCH ALLYN, INC. KLEENSPEC 590 SERIES DISP. VAGINAL SPECU 10/01/2014
-
-