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R-Group Intl.

FDA 510(k) & PMA Approved Devices — 7 products

Total Devices7

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K001233	ACTI-FLEX FLUID DELIVERY SYSTEM OR ACTI-FLEX F D S	FPA	2000-12-13	View
510(k)	K001599	ACTI-FLEX IV ADMINISTRATION SET	FPA	2000-09-18	View
510(k)	K993777	DISPOSABLE AND REUSABLE BALL AND LOOP ELECTRODES	HGI	2000-05-25	View
510(k)	K952470	ACTI-FLEX LOW, MEDIUM, RESCARE I, RESCARE II.	GCD	1995-11-28	View
510(k)	K954035	ACTI-FLEX ARTERIAL EXTENSION SET	CBT	1995-09-25	View
510(k)	K940319	R-GROUP INTERNATIONAL COILED LOW PRESSURE EXTENSION LINE	FPA	1994-11-10	View
510(k)	K913267	R-GROUP INTL. ONE WALL PUNCTURE NEEDLE	DRC	1992-06-05	View

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