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

Ambicare Health, Ltd.

FDA 510(k) & PMA Approved Devices — 1 products

Total Devices1
Categories1
Latest Approval2016-01-19
TypeNumberDevice NameCodeDate
510(k) K143713 Lustre PRO Light System GEX 2016-01-19 View