Medical Device Manufacturer · US , Placentia , CA

Watlow/Winona, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1986

Total

Cleared

Denied

Watlow/Winona, Inc. has 1 FDA 510(k) cleared medical devices. Based in Placentia, US.

Historical record: 1 cleared submissions from 1986 to 1986. Primary specialty: Neurology.

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

Watlow/Winona, 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 - Watlow/Winona, Inc.

1 devices

1-1 of 1