Medical Device Manufacturer · US , Mchenry , IL

Anritsu America Co. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1979

Total

Cleared

Denied

Anritsu America Co. has 2 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 2 cleared submissions from 1979 to 1981. Primary specialty: Neurology.

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

Anritsu America Co. 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 - Anritsu America Co.

2 devices

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