Medical Device Manufacturer · US , Danvers , MA

Infusion Technology Intl. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1994

Total

Cleared

Denied

Infusion Technology Intl. has 3 FDA 510(k) cleared medical devices. Based in Danvers, US.

Historical record: 3 cleared submissions from 1994 to 1995. Primary specialty: General Hospital.

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

Infusion Technology Intl. 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 - Infusion Technology Intl.

3 devices

1-3 of 3