Medical Device Manufacturer · US , South San Fransisco , CA

Ge Imatron - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2002

Total

Cleared

Denied

Ge Imatron has 1 FDA 510(k) cleared medical devices. Based in South San Fransisco, US.

Historical record: 1 cleared submissions from 2002 to 2002. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Ge Imatron

1 devices

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