• 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
-
191 to 200 of 500 Results *
 < 
 19 
 20 
 21 
 22 
 23 
 24 
 25 
 26 
 27 
 28 
 > 
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]
lifepak 12defiberllator/monitor series MEDTRONIC PHYSIO-CONTROL CORP. k002445 01/31/2001
noninvasive blood pressure measurement system UNIX ELECTRONIC CO. LTD. k002791 01/29/2001
the bioplate regid fixation bone plating system for cranomaxillofacial surgery BIOPLATE, INC. k002426 01/26/2001
modification to fluorotex ii surgical mesh BRIDGER BIOMED, INC. k003917 01/26/2001
powdered latex examination gloves with protein content labeling claim (200 micrograms or less) SELTOM PACIFIC SDN. BHD. k003934 01/26/2001
denlaser, model 800 CAO GROUP, INC. k003541 01/25/2001
dyract cem lci compomer DENTSPLY INTL. k003921 01/24/2001
a&d medical tm-2550/tm-2551/tm-2560 vital sensor monitor A & D ENGINEERING, INC. k002061 01/19/2001
trak back ii JOMED, INC. k003938 01/18/2001
vivid 7 with sonopac, model fb0008xx GE MEDICAL SYSTEMS, INC. k003931 01/18/2001

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