Medical Device Manufacturer · US , New Brunswick , NJ

Richmond Diagnostics, Inc.

1 submissions · 1 cleared · Since 1997

Total

Cleared

Denied

Richmond Diagnostics, Inc. — FDA 510(k) Submissions

Richmond Diagnostics, Inc. has submitted 1 FDA 510(k) premarket notifications since 1997, of which 1 received clearance as substantially equivalent to a predicate device.

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

1 devices

1–1 of 1

HEMATACHEK

K964452 · GLK Control, Hematocrit · Hematology

Feb 1997 106d

Richmond Diagnostics, Inc.

Richmond Diagnostics, Inc. — FDA 510(k) Submissions

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