Hankscraft Div. of Gerber Products Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hankscraft Div. of Gerber Products Co. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
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