Medical Device Manufacturer · US , Grand Junction , CO

Martin Dalsing - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1997

Total

Cleared

Denied

Martin Dalsing has 2 FDA 510(k) cleared medical devices. Based in Grand Junction, US.

Historical record: 2 cleared submissions from 1997 to 1997. Primary specialty: Ophthalmic.

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

Martin Dalsing 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 - Martin Dalsing

2 devices

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