The Prometheus Group is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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.
FDA 510(k) Regulatory Record - The Prometheus Group
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