Medical Device Manufacturer · US , Derwood , MD

Cell Ent., Inc.

1 submissions · 1 cleared · Since 1989
1
Total
1
Cleared
0
Denied

Cell Ent., Inc. — FDA 510(k) Submissions

Cell Ent., Inc. has submitted 1 FDA 510(k) premarket notifications since 1989, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Media And Components, Synthetic Cell And Tissue Culture . Use the specialty filter in the sidebar to narrow results.

1 devices
1–1 of 1
Filters
Filter by Specialty
All1 Pathology 1