Medical Device Manufacturer · US , Gainesville , FL

R-Group Intl. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1992

7

Total

7

Cleared

0

Denied

R-Group Intl. has 7 FDA 510(k) cleared medical devices. Based in Gainesville, US.

Historical record: 7 cleared submissions from 1992 to 2000. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by R-Group Intl. Filter by specialty or product code using the sidebar.

7 devices

1–7 of 7

ACTI-FLEX FLUID DELIVERY SYSTEM OR ACTI-FLEX F D S

K001233 · FPA Set, Administration, Intravascular · General Hospital

ACTI-FLEX IV ADMINISTRATION SET

K001599 · FPA Set, Administration, Intravascular · General Hospital

DISPOSABLE AND REUSABLE BALL AND LOOP ELECTRODES

K993777 · HGI Electrocautery, Gynecologic (and Accessories) · Obstetrics & Gynecology

ACTI-FLEX LOW, MEDIUM, RESCARE I, RESCARE II.

K952470 · GCD Connector, Catheter · General & Plastic Surgery

ACTI-FLEX ARTERIAL EXTENSION SET

K954035 · CBT Arterial Blood Sampling Kit · Anesthesiology

R-GROUP INTERNATIONAL COILED LOW PRESSURE EXTENSION LINE

K940319 · FPA Set, Administration, Intravascular · General Hospital

R-GROUP INTL. ONE WALL PUNCTURE NEEDLE

K913267 · DRC Trocar · Cardiovascular