Medical Device Manufacturer · US , Gaithersburg , MD

Eg &G Wallac - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1997

Total

Cleared

Denied

Eg &G Wallac has 1 FDA 510(k) cleared medical devices. Based in Gaithersburg, US.

Historical record: 1 cleared submissions from 1997 to 1997. Primary specialty: Chemistry.

Browse the FDA 510(k) cleared devices submitted by Eg &G Wallac Filter by specialty or product code using the sidebar.

Eg &G Wallac is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Eg &G Wallac

1 devices

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