Medical Device Manufacturer · US , Franktown , CO

Ansr Ent., Inc.

1 submissions · 1 cleared · Since 1988

Total

Cleared

Denied

Ansr Ent., Inc. — FDA 510(k) Submissions

Ansr Ent., Inc. has submitted 1 FDA 510(k) premarket notifications since 1988, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Manometer, Spinal-fluid . Use the specialty filter in the sidebar to narrow results.

1 devices

1–1 of 1

HYPODERMIC NEEDLE SHEATH HOLDER

K882405 · FMJ Manometer, Spinal-fluid · General Hospital

Jun 1988 19d

Ansr Ent., Inc.

Ansr Ent., Inc. — FDA 510(k) Submissions

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