Should Medical Apps Face Government Oversight?: Scientific American Apr 12 ’10 http://ow.ly/1yViv
AAMI Updates EtO Sterilization Guidance Document AAMI TIR15
AAMI Updates EtO Sterilization Guidance Document AAMI TIR15 http://ow.ly/1yxKk
STERIS System 1 Alternative System 1E Cleared by FDA
STERIS System 1 Alternative System 1E Cleared by FDA April 5, 2010 on STERIS System 1 updates webpage – http://ow.ly/1yvpf
FDA Requires Manufacturers to Include Info on Pediatric Populations
FDA Requires Device Manufacturers to Include Information on Pediatric Populations http://ow.ly/1vJpz
US Devicemakers Given Three Year Transition to IEC 60601-1
Devicemakers Given Three Years to Transition to New Standard From FDA News Devices & Diagnostic Letter March 29, 2010 Devicemakers may have to pay up to 40 percent more to test the safety and effectiveness of electronic devices now that
