Medical Device Manufacturer · US , Mchenry , IL

Intl. General Electric Co. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1981
1
Total
1
Cleared
0
Denied

Intl. General Electric Co. has 1 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 1 cleared submissions from 1981 to 1981. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Intl. General Electric Co. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Intl. General Electric Co.
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