Medical Device Manufacturer · US , Mchenry , IL

Vistek Corp. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1984

Total

Cleared

Denied

Vistek Corp. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 5 cleared submissions from 1984 to 1990. Primary specialty: General & Plastic Surgery.

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

Vistek 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 - Vistek Corp.

5 devices

1-5 of 5