Salter Labs - FDA 510(k) Cleared Devices

Salter Labs has 49 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.

Latest FDA clearance: Jul 2026. Active since 1978.

Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Airlife Finland OY as regulatory consultant.