Medical Device Manufacturer · US , Mchenry , IL

Medprobe Laboratories - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1982

Total

Cleared

Denied

Medprobe Laboratories has 4 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 4 cleared submissions from 1982 to 1983. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Medprobe Laboratories Filter by specialty or product code using the sidebar.

Medprobe Laboratories 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 - Medprobe Laboratories

4 devices

1-4 of 4