Medical Device Manufacturer · US , Mchenry , IL

Precision Cap Systems - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1983

Total

Cleared

Denied

Precision Cap Systems has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 7 cleared submissions from 1983 to 1983. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Precision Cap Systems Filter by specialty or product code using the sidebar.

Precision Cap Systems 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 - Precision Cap Systems

7 devices

1-7 of 7