Medical Device Manufacturer · US , Rockville , MD

Tournier-Bottu S.A. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1997

Total

Cleared

Denied

Tournier-Bottu S.A. has 1 FDA 510(k) cleared medical devices. Based in Rockville, US.

Historical record: 1 cleared submissions from 1997 to 1997. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Tournier-Bottu S.A. Filter by specialty or product code using the sidebar.

Tournier-Bottu S.A. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Tournier-Bottu S.A.

1 devices

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