R.H. Burton Co. - FDA 510(k) Cleared Devices
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.
19 devices
Cleared
Jun 07, 1993
BURTON H- BASE TABLE - MODEL 1990
Orthopedic
257d
Cleared
Apr 14, 1993
BURTON AUTOMATIC PROJECTOR - MODEL CP-40
Ophthalmic
203d
Cleared
Apr 14, 1993
BURTON SLIT LAMP - MODEL 850
Ophthalmic
203d
Cleared
Apr 14, 1993
BURTON TRIAL LENS SET
Ophthalmic
203d
Cleared
Apr 05, 1993
BURTON OPHTHALMIC STAND - MODEL XL3200
Ophthalmic
194d
Cleared
Apr 05, 1993
BURTON LENSMETER - MODEL 2021
Ophthalmic
194d
Cleared
Apr 05, 1993
BURTON APPLANATION TONOMETER - MODEL T850 & T1000
Ophthalmic
194d
Cleared
Apr 05, 1993
BURTON AUTO REFRACTOR/KERATOMETER - MODEL BARK-8
Ophthalmic
194d
Cleared
Apr 05, 1993
BURTON KERATOMETER - MODLE 2040
Ophthalmic
194d
Cleared
Apr 05, 1993
BURTON OPHTHALMIC EXAM UNIT - MODEL 2201
Ophthalmic
194d
Cleared
Apr 05, 1993
BURTON PROJECTOR HEAD - MODEL 6000-H
Ophthalmic
194d
Cleared
Apr 05, 1993
BURTON RADIUSGAUGE - MODEL 2030
Ophthalmic
194d