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 3 of 3 Results
ProductCode: FPA Applicant: R-GROUP INTL. Decision Date To: 05/23/2024
Results per Page
New Search  
Export all 3 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]
acti-flex fluid delivery system or acti-flex f d s R-GROUP INTL. K001233 12/13/2000
acti-flex iv administration set R-GROUP INTL. K001599 09/18/2000
r-group international coiled low pressure extension line R-GROUP INTL. K940319 11/10/1994
-
-