Medical Device Manufacturer · IE , Co. Tipperary

Techno-Path Manufacturing - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2017

Total

Cleared

Denied

Techno-Path Manufacturing has 1 FDA 510(k) cleared medical devices. Based in Co. Tipperary, IE.

Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Chemistry.

Browse the FDA 510(k) cleared devices submitted by Techno-Path Manufacturing Filter by specialty or product code using the sidebar.

Techno-Path Manufacturing is one of 45 FDA 510(k) medical device manufacturers from Ireland in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Techno-Path Manufacturing

1 devices

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