Medical Device Manufacturer · US , Great Neck, , NY

Myelotec, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1996

Total

Cleared

Denied

Myelotec, Inc. has 2 FDA 510(k) cleared medical devices. Based in Great Neck,, US.

Historical record: 2 cleared submissions from 1996 to 1998. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Myelotec, Inc.

2 devices

1-2 of 2