R-Group Intl.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K001233ACTI-FLEX FLUID DELIVERY SYSTEM OR ACTI-FLEX F D SDecember 13, 2000
K001599ACTI-FLEX IV ADMINISTRATION SETSeptember 18, 2000
K993777DISPOSABLE AND REUSABLE BALL AND LOOP ELECTRODESMay 25, 2000
K952470ACTI-FLEX LOW, MEDIUM, RESCARE I, RESCARE II.November 28, 1995
K954035ACTI-FLEX ARTERIAL EXTENSION SETSeptember 25, 1995
K940319R-GROUP INTERNATIONAL COILED LOW PRESSURE EXTENSION LINENovember 10, 1994
K913267R-GROUP INTL. ONE WALL PUNCTURE NEEDLEJune 5, 1992