• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(K) Premarket Notification

  • Print
  • Share
  • E-mail
-
271 to 280 of 493 Results
 < 
 27 
 28 
 29 
 30 
 31 
 32 
 33 
 34 
 35 
 36 
 > 
 
New Searchexport reports to excelExport to Excel | HelpHelp
Device Name
Sort by Device Name [A-Z]
Sort by Device Name [Z-A]
Applicant
Sort by PMA Number [0-9]
Sort by PMA Number [9-0]
510(K)
Number
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
Decision
Date
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
intrastent doublestrut paramount biliary endoprosthesis Intratherapeutics, Inc. k003450 12/07/2000
interplate c Rsb Spine, LLC k092070 10/06/2009
intellivue patient monitor, intellibridge module, models mp40, mp50, mp60, mp70, mp80, mp90, ec10, ec5 Philips Medizinsysteme Boeblingen GmbH, Cardiac AN k082583 02/25/2009
intellispace ecg Philips Health Care k120855 06/29/2012
insight plus 9000 phased array torso and pelvis coil Usa Instruments, Inc. k001209 06/01/2000
inpulse dental laser Incisive, LLC k011423 08/07/2001
improved try-in gel Sybron Dental Specialties, Inc. k001899 08/28/2000
immulite valproic acid, immulite 2000 valproic acid, catalog # lkva1, lkva5 & l2kva2, l2kva6 Diagnostic Products Corp. k000005 03/03/2000
immulite phenytoin, immulite 2000 phenytoin, catalog # lkpn1, lkpn5 & l2kpn2, l2kpn6 Diagnostic Products Corp. k000006 02/28/2000
immulite phenobarbital, models lkpb1, lkpb5 Diagnostic Products Corp. k000012 03/03/2000

-
-