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.

Spectrum Medical Technologies, Inc.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K963947 EPILASER NORMAL MODE RUBY LASERGEX1997-03-05 View
510(k) K955612 RD-1200H NORMAL MODE RUBY LASER SYSTEMGEX1996-07-09 View
510(k) K910422 MODEL RD-1200 RUBY LASER SYSTEMGEX1992-04-21 View
↑