Medical Device Manufacturer · US , San Antonio , TX

Viratest Intl., Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1994

Total

Cleared

Denied

Viratest Intl., Inc. has 3 FDA 510(k) cleared medical devices. Based in San Antonio, US.

Historical record: 3 cleared submissions from 1994 to 1996. Primary specialty: Microbiology.

Browse the FDA 510(k) cleared devices submitted by Viratest Intl., Inc. Filter by specialty or product code using the sidebar.

Viratest Intl., Inc. 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 - Viratest Intl., Inc.

3 devices

1-3 of 3