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.

Mehl/Biophile Intl., Inc.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K980753 CHROMOSCAN SCANNING SYSTEMGEX1998-06-29 View
510(k) K971814 IMPROVEMENTS TO THE MEHL RUBY LASERGEX1997-08-01 View
↑