Medical Device Manufacturer · US , Menomonee Falls , WI

Myo/Kinetic Systems, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1992

Total

Cleared

Denied

Myo/Kinetic Systems, Inc. has 8 FDA 510(k) cleared medical devices. Based in Menomonee Falls, US.

Historical record: 8 cleared submissions from 1992 to 1995. Primary specialty: Gastroenterology & Urology.

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

Myo/Kinetic Systems, 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 - Myo/Kinetic Systems, Inc.

8 devices

1-8 of 8