Medical Device Manufacturer · CH , Switzerland

Glaser Instruments AG - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1994

Total

Cleared

Denied

Glaser Instruments AG has 2 FDA 510(k) cleared medical devices. Based in Switzerland, CH.

Historical record: 2 cleared submissions from 1994 to 1994. Primary specialty: Ear, Nose, Throat.

Browse the FDA 510(k) cleared devices submitted by Glaser Instruments AG Filter by specialty or product code using the sidebar.

Glaser Instruments AG is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Glaser Instruments AG

2 devices

1-2 of 2