Medical Device Manufacturer · US , Wilmington , DE

Amalgam Rx, Inc.

1 submissions · 1 cleared · Since 2024
1
Total
1
Cleared
0
Denied

Amalgam Rx, Inc. — FDA 510(k) Submissions

Amalgam Rx, Inc. has submitted 1 FDA 510(k) premarket notifications since 2024, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Calculator, Drug Dose . Use the specialty filter in the sidebar to narrow results.

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