Physio Technology, Inc.
Physio Technology, Inc. holds FDA 510(k) medical device clearances, first cleared 1984, most recent 1988.
Top product codes for Physio Technology, Inc.
Recent clearances by Physio Technology, Inc.
- K883893 — OMNISOUND(TM) 3000
- K874076 — MODIFIED OMNISTIM(TM) ELECTRICAL MUSCLE STIMULATOR
- K861039 — OMNIVAC (VACUUM ELECTRODE SYSTEM)
- K850850 — AUTOMOVE/OMNISTIM IV-ELECTRICAL MUSCLE STIMULATOR
- K850851 — G5 APPARATUS T, K1, K3 & THE PRESIDENT MODEL'S
- K850849 — MYOMETER EMG BIOFEEDBACK DEVICE
- K843351 — OMNISTIM II COMBIN. THERAPY SYS
- K843372 — OMNISOUND THERAPY UNIT
- K841874 — MEGA PULSE THERAPY UNIT
- K841278 — OMNISTIM III INTERFERENTIAL THERAPY
Data sourced from openFDA. This site is unofficial and independent of the FDA.