Medical Device Manufacturer · US , Mchenry , IL

Staodynamics, Inc. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 1979

Total

Cleared

Denied

Staodynamics, Inc. has 14 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 14 cleared submissions from 1979 to 1985. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Staodynamics, Inc. Filter by specialty or product code using the sidebar.

Staodynamics, 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 - Staodynamics, Inc.

14 devices

1-12 of 14

Cleared Jun 24, 1985

TENS-AID STERILE ELECTRODES FOR POST-OP TENS

K852298 · GXY

Neurology · 26d

Cleared Feb 25, 1985

TENS-AID PREMIUM ELECTRODES

Physical Medicine · 82d

General Hospital · 84d

Cleared Feb 26, 1980

POINT LOCATOR STIMULATOR

K792529 · BWJ

General Hospital · 81d

Cleared Feb 05, 1980

ELECTRICAL MUSCLE STIMULATOR (EMS)

K800068 · IPF

Physical Medicine · 25d

PORTABLE PULSE GALVANIC STIMULATOR

K791087 · IPF

Physical Medicine · 122d

Staodynamics, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Staodynamics, Inc.

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