Medical Device Manufacturer · US , Norcross , GA

Immucor, Inc.

3 submissions · 3 cleared · Since 1991
3
Total
3
Cleared
0
Denied

Immucor, Inc. — FDA 510(k) Submissions

Immucor, Inc. has submitted 3 FDA 510(k) premarket notifications since 1991, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Antigen, Iha, Cytomegalovirus . Use the specialty filter in the sidebar to narrow results.

3 devices
1–3 of 3
Filters
Filter by Specialty
All3 Microbiology 3