Medical Device Manufacturer · US , San Diego , CA

Metamed, Inc.

1 submissions · 1 cleared · Since 1994

Total

Cleared

Denied

Metamed, Inc. — FDA 510(k) Submissions

Metamed, Inc. has submitted 1 FDA 510(k) premarket notifications since 1994, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Controller, Infusion, Intravascular, Electronic . Use the specialty filter in the sidebar to narrow results.

1 devices

1–1 of 1

UNIVERSAL CONTROLLER, MODEL 100

K934543 · LDR Controller, Infusion, Intravascular, Electronic · General Hospital

Mar 1994 194d

Metamed, Inc.

Metamed, Inc. — FDA 510(k) Submissions

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