• 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
-
11 to 20 of 185 Results
ProductCode: FPA Applicant: Y Decision Date To: 08/29/2016
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
Results per Page
New Search  
Export all 185 Records to ExcelExport to Excel | Download Files | More About 510(k)
Device Name
Sort by Device Name [A-Z]
Sort by Device Name [Z-A]
Applicant
Sort by Applicant [A-Z]
Sort by Applicant [Z-A]
510(K)
Number
Sort by 510(k) Number [0-9]
Sort by 510(k) Number [9-0]
Decision
Date
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
burette intravenous admin. sets. Y K780130 02/21/1978
controlled release infusion system(cris) Y K852488 06/27/1985
cris adapted with volume limiting bag Y K864164 12/16/1986
cris adapter Y K883986 02/24/1989
ez administration set Y K931550 01/10/1994
infusion set-52-05-1 20 drops-mi vol Y K833033 11/07/1983
intravascular administration set Y K790582 05/29/1979
intravascular administration set Y K820278 02/18/1982
ivac 52-99-0 unvented & 52-99-1 vented vol. infusi Y K844937 01/25/1985
ivac 59 series universal set w/ anti-free flow val Y K925228 07/30/1993
-
-