Medical Device Manufacturer · US , Mchenry , IL

Grass Instrument Co. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1977

Total

Cleared

Denied

Grass Instrument Co. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 6 cleared submissions from 1977 to 2002. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Grass Instrument Co. Filter by specialty or product code using the sidebar.

Grass Instrument Co. 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 - Grass Instrument Co.

6 devices

1-6 of 6