Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Dayton Mfg. Co.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K870072 SUMMIT OPTICS CONTACT LENS REMOVERKYE1987-02-12 View
510(k) K870164 SUMMIT OPTICS SOFT CONTACT LENS CASELRX1987-02-10 View
↑