Medical Device Manufacturer · US , Mchenry , IL

Wilton Webster Laboratories - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1978
2
Total
2
Cleared
0
Denied

Wilton Webster Laboratories has 2 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 2 cleared submissions from 1978 to 1979. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Wilton Webster Laboratories Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Wilton Webster Laboratories

2 devices
1-2 of 2
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