Medical Device Manufacturer · US , Walker , MI

Physio Technology, Inc. - FDA 510(k) Cleared Devices

10 submissions · 9 cleared · Since 1984

Total

Cleared

Denied

Physio Technology, Inc. has 9 FDA 510(k) cleared physical medicine devices. Based in Walker, US.

Historical record: 9 cleared submissions from 1984 to 1988.

Browse the complete list of FDA 510(k) cleared physical medicine devices from this manufacturer. Filter by specialty or product code using the sidebar.

Physio Technology, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Physio Technology, Inc.

10 devices

1-10 of 10

Cleared Nov 01, 1988

OMNISOUND(TM) 3000

K883893 · IMG

Physical Medicine · 48d

Cleared Jan 04, 1988

MODIFIED OMNISTIM(TM) ELECTRICAL MUSCLE STIMULATOR

K874076 · IPF

Physical Medicine · 90d

Cleared Sep 26, 1986

OMNIVAC (VACUUM ELECTRODE SYSTEM)

K861039 · LIH

Neurology · 192d

Cleared Jul 01, 1985

AUTOMOVE/OMNISTIM IV-ELECTRICAL MUSCLE STIMULATOR

K850850 · IPF

Physical Medicine · 122d

Cleared Jun 25, 1985

G5 APPARATUS T, K1, K3 & THE PRESIDENT MODEL'S

K850851 · ISA

Physical Medicine · 116d

Cleared May 31, 1985

MYOMETER EMG BIOFEEDBACK DEVICE

K850849 · HCC

Neurology · 91d

Cleared Sep 18, 1984

OMNISTIM II COMBIN. THERAPY SYS

K843351 · IMG

Physical Medicine · 22d

Cleared Sep 18, 1984

OMNISOUND THERAPY UNIT

K843372 · IMI

Physical Medicine · 21d

Cleared May 31, 1984

MEGA PULSE THERAPY UNIT

K841874 · IMJ

Physical Medicine · 24d

Cleared Apr 24, 1984

OMNISTIM III INTERFERENTIAL THERAPY

K841278 · IPF

Physical Medicine · 27d

Physio Technology, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Physio Technology, Inc.

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