Medical Device Manufacturer · US , Morton Grove , IL

Haemoscope Corp. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1989

Total

Cleared

Denied

Haemoscope Corp. has 7 FDA 510(k) cleared medical devices. Based in Morton Grove, US.

Historical record: 7 cleared submissions from 1989 to 2007. Primary specialty: Hematology.

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

Haemoscope 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 - Haemoscope Corp.

7 devices

1-7 of 7