Medical Device Manufacturer · US , St. Louis , MO

The Lighthouse For the Blind, Inc. - FDA 510(k) Cleared Devices

2 submissions · 1 cleared · Since 1992
2
Total
1
Cleared
0
Denied

The Lighthouse For the Blind, Inc. has 1 FDA 510(k) cleared medical devices. Based in St. Louis, US.

Historical record: 1 cleared submissions from 1992 to 1994. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by The Lighthouse For the Blind, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - The Lighthouse For the Blind, Inc.

2 devices
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