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: FMJ 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
SMITHS MEDICAL, INC. HYPODERMIC NEEDLE=PRO EDGE DEVICE 05/21/2015
SMITHS MEDICAL, INC. HYPODERMINC NEEDLE-PRO EDGE DEVICE 05/21/2015
SMITHS MEDICAL MD, INC. HYPODERMIC NEEDLE-PRO EDGE DEVICE 05/21/2015
SMITHS MEDICAL, INC. HYPODERMIC NEEDLE-PRO DEVICE 05/11/2015
SMITHS MEDICAL INC HYPODERMIC NEEDLE-PRO DEVICE 04/22/2015
SMITHS MEDICAL INC HYPODERMIC NEEDLE-PRO DEVICE 04/01/2015
SMITHS MEDICAL, INC HYPODERMIC NEEDLE-PRO DEVICE 03/03/2015
SMITHS MEDICAL, INC HYPODERMIC NEEDLE-PRO DEVICE 03/03/2015
-
-