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.

The LE Blanc Corp.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K885137 ASTRO TRACE (MODEL AT-02)DSA1989-03-15 View
510(k) K884592 ASTRO TRACE (MODEL AT-01)DSA1989-03-02 View
↑