Medical Device Manufacturer · US , Wayland , MA

Embryotech Laboratories, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1998

Total

Cleared

Denied

Embryotech Laboratories, Inc. has 2 FDA 510(k) cleared medical devices. Based in Wayland, US.

Historical record: 2 cleared submissions from 1998 to 2001. Primary specialty: Hematology.

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

Embryotech Laboratories, 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 - Embryotech Laboratories, Inc.

2 devices

1-2 of 2