Medical Device Manufacturer · US , Washington , DC

Lifetrac, Inc.

1 submissions · 1 cleared · Since 1985

Total

Cleared

Denied

Lifetrac, Inc. — FDA 510(k) Submissions

Lifetrac, Inc. has submitted 1 FDA 510(k) premarket notifications since 1985, of which 1 received clearance as substantially equivalent to a predicate device.

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

1 devices

1–1 of 1

CEKK-ADHESIVE MATRIX-MULTIPLE WELL PLATE CAM-PLATE

K854724 · KIZ Dish, Tissue Culture · Pathology

Dec 1985 21d

Lifetrac, Inc.

Lifetrac, Inc. — FDA 510(k) Submissions

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