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FDA 510(k) Applications Submitted by RICHARD M HORTON
FDA 510(k) Number
Submission Date
Device Name
Applicant
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
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