The Prometheus Group - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
The Prometheus Group has 11 FDA 510(k) cleared medical devices. Based in Portsmouth, US.
Historical record: 11 cleared submissions from 1991 to 2016. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by The Prometheus Group Filter by specialty or product code using the sidebar.
11 devices
Cleared
Apr 15, 2016
Morpheus RealTime Ultrasound, Pathway RealTime Ultrasound, QuickScan Bladder...
Radiology
23d
Cleared
May 23, 2003
PATHWAY STM-10 PELVIC FLOOR STIMULATOR
Gastroenterology & Urology
137d
Cleared
Feb 19, 2003
PATHWAY CTS2000 PELVIC FLOOR TRAINING SYSTEM
Gastroenterology & Urology
89d
Cleared
Jul 31, 2000
PATHWAY CTS 2000 PELVIC FLOOR TRAINING SYSTEM, MODEL PATHWAY CTS 2000
Gastroenterology & Urology
76d
Cleared
Feb 22, 2000
PATHWAY VAGINAL EMG/STIM PERINEOMETER SENSOR, PATHWAY ANAL EMG/STIM...
Gastroenterology & Urology
90d
Cleared
Dec 22, 1997
PATHWAY VAGINAL/RECTAL PERINEOMETER PROBE
Gastroenterology & Urology
59d
Cleared
Dec 17, 1997
PATHWAY ELECTROMYOGRAPH
Neurology
90d
Cleared
Jan 16, 1997
PATHWAY ELECTROMYOGRAPH MODEL PATHWAY II/MR-10/MR-15/MR-20/MR-25
Gastroenterology & Urology
346d
Cleared
Aug 07, 1996
PATHWAY ELECTROMYOGRAPH MODEL TR-10 & TR-20
Neurology
163d
Cleared
Jun 13, 1996
SYNERGY PLUS
Neurology
108d
Cleared
Apr 18, 1991
PATHWAY II ELECTROMYOGRAPH
Neurology
477d