Medical Device Manufacturer · US , New York , NY

Heartware Intl. Corp. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1989

Total

Cleared

Denied

Heartware Intl. Corp. has 4 FDA 510(k) cleared medical devices. Based in New York, US.

Historical record: 4 cleared submissions from 1989 to 1993. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Heartware Intl. Corp.

4 devices

1-4 of 4