Medical Device Manufacturer · US , Silver Spring , MD

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

1 submissions · 1 cleared · Since 2014

Total

Cleared

Denied

Anthrotronix, Inc. has 1 FDA 510(k) cleared medical devices. Based in Silver Spring, US.

Historical record: 1 cleared submissions from 2014 to 2014. Primary specialty: Neurology.

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

Anthrotronix, Inc. is one of 5120 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

Anthrotronix, Inc. — FDA 510(k) Products and Clearance History

1 devices

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