# R.H. Burton Co.

- Location (FDA's records): Grove City, OH
- FDA decisions: 19 (1992–1993): 19 510(k) clearances
- Product codes: HJO (4), HLM (3), HMF (2), HKO (2), HPC (2), HOD (1), HKX (1), HOS (1), HJB (1), HRJ (1), HRX (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K924773: Burton H- Base Table - Model 1990 (Jun 7, 1993)
- K924774: Burton Automatic Projector - Model CP-40 (Apr 14, 1993)
- K924783: Burton Slit Lamp - Model 850 (Apr 14, 1993)
- K924786: Burton Trial Lens Set (Apr 14, 1993)
- K924780: Burton Ophthalmic Exam Unit - Model 2201 (Apr 5, 1993)
- K924778: Burton Auto Refractor/Keratometer - Model Bark-8 (Apr 5, 1993)
- K924785: Burton Radiusgauge - Model 2030 (Apr 5, 1993)
- K924776: Burton Lensmeter - Model 2021 (Apr 5, 1993)

Source page: https://510kreport.com/company/rh-burton