Chattanooga Group, Inc.

FDA 510(k) & PMA Approved Devices — 70 products

Total Devices70

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K011243	CHATTANOOGA DRY HEAT WHIRLPOOL, MODEL 2000	LSB	2001-07-06	View
510(k)	K982324	VECTRA PRO MODELS 2 AND 4	GZJ	1999-02-01	View
510(k)	K982321	VECTRA STIM MODELS 200 AND 400	GZJ	1999-02-01	View
510(k)	K982317	VECTRA COMBO	IMG	1999-02-01	View
510(k)	K982828	FORTE, MODELS CPS 400 STIM, CPS 200 STIM	IPF	1998-11-06	View
510(k)	K982830	FORTE, MODELS CPS 400 COMBO, CPS 200 COMBO	IMG	1998-11-06	View
510(k)	K982829	FORTE, MODEL CPS ULTRASOUND	IMI	1998-11-06	View
510(k)	K980718	PARA-CARE	IMC	1998-03-27	View
510(k)	K974497	INTELECT	GZJ	1998-01-23	View
510(k)	K973024	INTELECT LEGEND ULTRASOUND	IMI	1997-11-10	View
510(k)	K972487	EMG RETRAINER	HCC	1997-09-26	View
510(k)	K953614	FORTE	IMG	1995-10-27	View
510(k)	K953615	FORTE ES-400	IPF	1995-10-27	View
510(k)	K951746	FORTE CB	IMG	1995-06-21	View
510(k)	K942796	PRESSSION S III	JOW	1995-03-24	View
510(k)	K940759	FORTE ES	GZI	1995-03-16	View
510(k)	K941561	FORTE US	IMG	1994-06-20	View
510(k)	K935324	THERAPEUTIC ULTRASOUND AND STIMULATOR	GZJ	1994-05-26	View
510(k)	K940180	FORTE US	IMG	1994-04-15	View
510(k)	K935271	THERAPEUTIC ULTRASOUND AND STIMULATOR	IMG	1994-02-02	View