Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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
-
1 to 4 of 4 Results
ProductCode: FPA Applicant: CRITICAL DEVICE CORP. Decision Date To: 04/23/2024
Results per Page
New Search  
Export all 4 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]
mps gravity flow control set CRITICAL DEVICE CORP. K983926 01/20/1999
nima needleless injectionsite master adapter with posiflow positive displacement feature, and i.v. sets CRITICAL DEVICE CORP. K964918 04/14/1997
nima needleless injectionsite master adapter and i.v. set CRITICAL DEVICE CORP. K964812 02/10/1997
nima (needleless injectionsite master adapter) & i.v. set CRITICAL DEVICE CORP. K952852 02/16/1996
-
-