R.H. Burton Co.
R.H. Burton Co. holds FDA 510(k) medical device clearances, first cleared 1992, most recent 1993.
Top product codes for R.H. Burton Co.
Recent clearances by R.H. Burton Co.
- K924773 — BURTON H- BASE TABLE - MODEL 1990
- K924774 — BURTON AUTOMATIC PROJECTOR - MODEL CP-40
- K924783 — BURTON SLIT LAMP - MODEL 850
- K924786 — BURTON TRIAL LENS SET
- K924771 — BURTON OPHTHALMIC STAND - MODEL XL3200
- K924776 — BURTON LENSMETER - MODEL 2021
- K924777 — BURTON APPLANATION TONOMETER - MODEL T850 & T1000
- K924778 — BURTON AUTO REFRACTOR/KERATOMETER - MODEL BARK-8
- K924779 — BURTON KERATOMETER - MODLE 2040
- K924780 — BURTON OPHTHALMIC EXAM UNIT - MODEL 2201
- K924784 — BURTON PROJECTOR HEAD - MODEL 6000-H
- K924785 — BURTON RADIUSGAUGE - MODEL 2030
- K924788 — BURTON LENSMETER
- K924790 — BURTON AUTO REFRACTOR - MODEL BAR-7
- K924770 — BURTON HAND HELD SLIT LAMP - MODEL SL750
- K924782 — BURTON SLIT LAMP - MODEL 2000
- K924787 — BURTON SLIT LAMP
- K922242 — 910T MONTORIZED INSTRUMENT TABLE
- K920571 — TRIAL LENS SET
Data sourced from openFDA. This site is unofficial and independent of the FDA.