Medical Device Manufacturer · US , Mchenry , IL

Schlosser Alberti Co. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1979

Total

Cleared

Denied

Schlosser Alberti Co. has 2 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 2 cleared submissions from 1979 to 1979. Primary specialty: Obstetrics & Gynecology.

Browse the FDA 510(k) cleared devices submitted by Schlosser Alberti Co. Filter by specialty or product code using the sidebar.

Schlosser Alberti Co. 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 - Schlosser Alberti Co.

2 devices

1-2 of 2