• 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
-
91 to 100 of 489 Results
ProductCode: FOZ Decision Date To: 01/23/2022
 < 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 > 
Results per Page
New Search  
Export all 489 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]
modified intravenous catheter SAFEGUARD NEEDLE CO. K896813 10/19/1990
heparin iv flush syringe, 10 u/ml \ ROCAP DIV. OF SABRATEK CORP. K990390 12/10/1999
rocap heparin iv flush syringe, 100u/ml ROCAP DIV. OF SABRATEK CORP. K990308 12/10/1999
normal saline flush syringe ROCAP DIV. OF SABRATEK CORP. K984614 05/27/1999
vanishpoint i.v. catheter RETRACTABLE TECHNOLOGIES, INC. K081420 11/07/2008
vanishpoint i.v. catheter RETRACTABLE TECHNOLOGIES, INC. K051355 09/23/2005
syrigene pre-filled syringe REGULATORY & MARKETING SERVICES, INC. K935669 02/18/1994
injection sealing cap 13791 QUINTON, INC. K830541 08/08/1983
luer locking adapter(material change) QUINTON, INC. K840815 11/08/1984
quinton white sealing cap QUINTON, INC. K850369 02/15/1985
-
-