Medical Device Manufacturer · US , Mchenry , IL

Hankscraft Div. of Gerber Products Co. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1979

Total

Cleared

Denied

Hankscraft Div. of Gerber Products Co. has 2 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 2 cleared submissions from 1979 to 1985. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Hankscraft Div. of Gerber Products Co. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Hankscraft Div. of Gerber Products Co.

2 devices

1-2 of 2