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.

M/S Midland Latex Products , Ltd.

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

Total Devices1
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K982114 LOPRO SILICONISED LOW PROTEIN POWDERFREE LATEX EXAMINATION GLOVESLYY1999-01-21 View
↑