• 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
-
61 to 70 of 490 Results
ProductCode: FOZ Decision Date To: 01/23/2022
 < 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 > 
Results per Page
New Search  
Export all 490 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]
deseret multilumen subclavian jugular PARKE-DAVIS CO. K840355 03/19/1984
deseret subclavian jugular cath. set PARKE-DAVIS CO. K834227 03/19/1984
deseret infant central venous cathe- PARKE-DAVIS CO. K840116 03/22/1984
luer locking adapter(material change) QUINTON, INC. K840815 11/08/1984
deseret dentral line catheter PARKE-DAVIS CO. K844219 11/28/1984
deseret subclavian jugular catheter set PARKE-DAVIS CO. K844113 11/28/1984
deseret intravascular catheter PARKE-DAVIS CO. K843033 12/03/1984
erythrocath umbilical catheter CARDIOSEARCH, INC. K841880 01/14/1985
quinton white sealing cap QUINTON, INC. K850369 02/15/1985
eyrthrocath double-lumen central venous CARDIOSEARCH, INC. K842133 02/19/1985
-
-