Medical Device Manufacturer · US , Walker , MI

Vitalog Corp. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1981

Total

Cleared

Denied

Vitalog Corp. has 4 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 4 cleared submissions from 1981 to 1988. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Vitalog Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Vitalog Corp.

4 devices

1-4 of 4