The Prometheus Group
The Prometheus Group holds FDA 510(k) medical device clearances, first cleared 1991, most recent 2016.
Top product codes for The Prometheus Group
Recent clearances by The Prometheus Group
- K160792 — Morpheus RealTime Ultrasound, Pathway RealTime Ultrasound, QuickScan Bladder Ultrasound
- K030039 — PATHWAY STM-10 PELVIC FLOOR STIMULATOR
- K023906 — PATHWAY CTS2000 PELVIC FLOOR TRAINING SYSTEM
- K001515 — PATHWAY CTS 2000 PELVIC FLOOR TRAINING SYSTEM, MODEL PATHWAY CTS 2000
- K993976 — PATHWAY VAGINAL EMG/STIM PERINEOMETER SENSOR, PATHWAY ANAL EMG/STIM PERINEOMETER SENSOR
- K974036 — PATHWAY VAGINAL/RECTAL PERINEOMETER PROBE
- K973537 — PATHWAY ELECTROMYOGRAPH
- K960508 — PATHWAY ELECTROMYOGRAPH MODEL PATHWAY II/MR-10/MR-15/MR-20/MR-25
- K960761 — PATHWAY ELECTROMYOGRAPH MODEL TR-10 & TR-20
- K960762 — SYNERGY PLUS
- K897132 — PATHWAY II ELECTROMYOGRAPH
Data sourced from openFDA. This site is unofficial and independent of the FDA.