Medical Device Manufacturer · US , Highland Park , IL

Pearl Instruments Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1989

Total

Cleared

Denied

Pearl Instruments Corp. has 2 FDA 510(k) cleared medical devices. Based in Highland Park, US.

Historical record: 2 cleared submissions from 1989 to 1990. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Pearl Instruments Corp. Filter by specialty or product code using the sidebar.

Pearl Instruments Corp. 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 - Pearl Instruments Corp.

2 devices

1-2 of 2