Medical Device Manufacturer · IL , Tirat Carmel

MeMed Diagnostics, Ltd.

3 submissions · 3 cleared · Since 2021
3
Total
3
Cleared
0
Denied

MeMed Diagnostics, Ltd. — FDA 510(k) Submissions

MeMed Diagnostics, Ltd. has submitted 3 FDA 510(k) premarket notifications since 2021, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Immunoassay For Host Biomarkers Of Infection . Use the specialty filter in the sidebar to narrow results.

3 devices
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All3 Microbiology 3