Medical Device Manufacturer · US , Bothell , WA

Microprobe Corp. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1992

Total

Cleared

Denied

Microprobe Corp. has 6 FDA 510(k) cleared medical devices. Based in Bothell, US.

Historical record: 6 cleared submissions from 1992 to 1993. Primary specialty: Microbiology.

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

Microprobe 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 - Microprobe Corp.

6 devices

1-6 of 6