Medical Device Manufacturer · BR , Sao Paulo-Sp

Timpel, Inc. - FDA 510(k) Cleared Devices

1 submissions · 0 cleared · Since 2018

Total

Cleared

Denied

Timpel, Inc. has 0 FDA 510(k) cleared medical devices. Based in Sao Paulo-Sp, BR.

Active since 2018. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Timpel, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Timpel, Inc.

1 devices

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