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.

Marvic Interpharma, Inc.

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

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K854223 VES-TEC/VES-MATICCKB1986-04-04 View
510(k) K854222 DIESSE RF TEST KITDHR1986-02-06 View
510(k) K854221 DIESSE CRP TEST KITDCK1985-11-25 View
↑