Medical Device Manufacturer · US , Orange , CA

Kerrhawe SA - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2012

Total

Cleared

Denied

Kerrhawe SA has 1 FDA 510(k) cleared medical devices. Based in Orange, US.

Historical record: 1 cleared submissions from 2012 to 2012. Primary specialty: Dental.

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

Kerrhawe SA 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 - Kerrhawe SA

1 devices

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