The Prometheus Group
FDA 510(k) medical device clearances.
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.