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The Prometheus Group

FDA 510(k) & PMA Approved Devices — 11 products

Total Devices11

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K160792	Morpheus RealTime Ultrasound, Pathway RealTime Ultrasound, QuickScan Bladder Ultrasound	IYO	2016-04-15	View
510(k)	K030039	PATHWAY STM-10 PELVIC FLOOR STIMULATOR	KPI	2003-05-23	View
510(k)	K023906	PATHWAY CTS2000 PELVIC FLOOR TRAINING SYSTEM	KPI	2003-02-19	View
510(k)	K001515	PATHWAY CTS 2000 PELVIC FLOOR TRAINING SYSTEM, MODEL PATHWAY CTS 2000	KPI	2000-07-31	View
510(k)	K993976	PATHWAY VAGINAL EMG/STIM PERINEOMETER SENSOR, PATHWAY ANAL EMG/STIM PERINEOMETER SENSOR	KPI	2000-02-22	View
510(k)	K974036	PATHWAY VAGINAL/RECTAL PERINEOMETER PROBE	HIR	1997-12-22	View
510(k)	K973537	PATHWAY ELECTROMYOGRAPH	HCC	1997-12-17	View
510(k)	K960508	PATHWAY ELECTROMYOGRAPH MODEL PATHWAY II/MR-10/MR-15/MR-20/MR-25	HIR	1997-01-16	View
510(k)	K960761	PATHWAY ELECTROMYOGRAPH MODEL TR-10 & TR-20	HCC	1996-08-07	View
510(k)	K960762	SYNERGY PLUS	HCC	1996-06-13	View
510(k)	K897132	PATHWAY II ELECTROMYOGRAPH	HCC	1991-04-18	View

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