FDA 510(k) Applications Submitted by THE PROMETHEUS GROUP

FDA 510(k) Number	Submission Date	Device Name	Applicant
K023906	11/22/2002	PATHWAY CTS2000 PELVIC FLOOR TRAINING SYSTEM	THE PROMETHEUS GROUP
K160792	03/23/2016	Morpheus RealTime Ultrasound, Pathway RealTime Ultrasound, QuickScan Bladder Ultrasound	THE PROMETHEUS GROUP
K030039	01/06/2003	PATHWAY STM-10 PELVIC FLOOR STIMULATOR	THE PROMETHEUS GROUP
K960761	02/26/1996	PATHWAY ELECTROMYOGRAPH MODEL TR-10 & TR-20	THE PROMETHEUS GROUP
K973537	09/18/1997	PATHWAY ELECTROMYOGRAPH	THE PROMETHEUS GROUP
K001515	05/16/2000	PATHWAY CTS 2000 PELVIC FLOOR TRAINING SYSTEM, MODEL PATHWAY CTS 2000	THE PROMETHEUS GROUP
K974036	10/24/1997	PATHWAY VAGINAL/RECTAL PERINEOMETER PROBE	THE PROMETHEUS GROUP
K993976	11/24/1999	PATHWAY VAGINAL EMG/STIM PERINEOMETER SENSOR, PATHWAY ANAL EMG/STIM PERINEOMETER SENSOR	THE PROMETHEUS GROUP
K960762	02/26/1996	SYNERGY PLUS	THE PROMETHEUS GROUP
K960508	02/05/1996	PATHWAY ELECTROMYOGRAPH MODEL PATHWAY II/MR-10/MR-15/MR-20/MR-25	THE PROMETHEUS GROUP