Medical Device Manufacturer · FI , Finland

Lasermatic OY - FDA 510(k) Cleared Devices

2 submissions · 1 cleared · Since 1988

Total

Cleared

Denied

Lasermatic OY has 1 FDA 510(k) cleared medical devices. Based in Finland, FI.

Historical record: 1 cleared submissions from 1988 to 1989. Primary specialty: Ear, Nose, Throat.

Browse the FDA 510(k) cleared devices submitted by Lasermatic OY Filter by specialty or product code using the sidebar.

Lasermatic OY is one of 32 FDA 510(k) medical device manufacturers from Finland in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Lasermatic OY

2 devices

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