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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