Medical Device Manufacturer · US , Mchenry , IL

Curomatic, Inc. - FDA 510(k) Cleared Devices

2 submissions · 1 cleared · Since 1978

Total

Cleared

Denied

Curomatic, Inc. has 1 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 1 cleared submissions from 1978 to 1979. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Curomatic, Inc. Filter by specialty or product code using the sidebar.

Curomatic, Inc. 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 - Curomatic, Inc.

2 devices

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