Medical Device Manufacturer · US , Minneapolis , MN

Midwest Eye Laboratories, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1991
2
Total
2
Cleared
0
Denied

Midwest Eye Laboratories, Inc. has 2 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 2 cleared submissions from 1991 to 1991. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Midwest Eye Laboratories, Inc. Filter by specialty or product code using the sidebar.

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