Medical Device Manufacturer · US , Minneapolis , MN

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

1 submissions · 1 cleared · Since 1993

Total

Cleared

Denied

Ergometrix, Inc. has 1 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 1 cleared submissions from 1993 to 1993. Primary specialty: Cardiovascular.

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

1 devices

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