• 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
-
291 to 300 of 500 Results *
 < 
 29 
 30 
 31 
 32 
 33 
 34 
 35 
 36 
 37 
 38 
 > 
results per page
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]
pm-8000 express patient monitor, model pm-8000 express SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD k053193 05/18/2006
cobas integra glucose hk gen. 3 test system ROCHE DIAGNOSTICS CORP. k061048 05/17/2006
iqmark ez stress BRENTWOOD MEDICAL TECHNOLOGY CORP. k052898 03/28/2006
liberty glucose control solution LIBERTY HEALTHCARE GROUP, INC. k060481 03/09/2006
codman hakim programmable valve w/wo siphonguard Codman & Shurtleff, Inc. k053107 01/19/2006
tangors polyaxial system ULRICH GMBH & CO. KG k052385 12/27/2005
nexa bone screw system NEXA ORTHOPEDICS, INC. k053394 12/14/2005
corolene PETERS SURGICAL k052701 12/13/2005
achieva, intera and panorama 1.0 release 2-series PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. k052078 09/07/2005
miot plating system ORTHOFIX SRL k051945 09/06/2005

*   The maximum 500 records meeting your search criteria returned. Please narrow your search.
-
-