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FDA 510(k) Applications Submitted by R-GROUP INTL.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K993777
11/08/1999
DISPOSABLE AND REUSABLE BALL AND LOOP ELECTRODES
R-GROUP INTL.
K001233
04/17/2000
ACTI-FLEX FLUID DELIVERY SYSTEM OR ACTI-FLEX F D S
R-GROUP INTL.
K001599
05/24/2000
ACTI-FLEX IV ADMINISTRATION SET
R-GROUP INTL.
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