Medical Device Manufacturer · US , Grove City , OH

R.H. Burton Co. - FDA 510(k) Cleared Devices

19 submissions · 19 cleared · Since 1992
19
Total
19
Cleared
0
Denied

R.H. Burton Co. has 19 FDA 510(k) cleared ophthalmic devices. Based in Grove City, US.

Historical record: 19 cleared submissions from 1992 to 1993.

Browse the complete list of FDA 510(k) cleared ophthalmic devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - R.H. Burton Co.
19 devices
1-12 of 19
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