Vitalograph , Ltd. - FDA 510(k) Cleared Devices

Vitalograph , Ltd. has 17 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.

Latest FDA clearance: Dec 2025. Active since 1979.

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 ProMedic Consulting, LLC as regulatory consultant.