Medical Device Manufacturer · US , Lancaster , PA

The Timeter Group - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1985

Total

Cleared

Denied

The Timeter Group has 4 FDA 510(k) cleared medical devices. Based in Lancaster, US.

Historical record: 4 cleared submissions from 1985 to 1987. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by The Timeter Group Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - The Timeter Group

4 devices

1-4 of 4