Myo/Kinetic Systems, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
FDA 510(k) Regulatory Record - Myo/Kinetic Systems, Inc. Gastroenterology & Urology ✕
4 devices
Cleared
Jul 14, 1995
TE-800 PELVIC FLOOR EXERCISER
Gastroenterology & Urology
221d
Cleared
Apr 12, 1995
TS-700P CONTROL XP ELECTRICAL STIMULATOR
Gastroenterology & Urology
163d
Cleared
Mar 08, 1995
URO-GRAM CYSTOMRTROGRAM WITH UROFLOWMETRY
Gastroenterology & Urology
148d
Cleared
Apr 18, 1994
UROGRAM CYSTOMETROGRAM
Gastroenterology & Urology
119d