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.

Kleartex Sdn Bhd

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K904361 KLEARTEX LATEX SURGEONS GLOVESKGO1990-12-07 View
510(k) K890975 PATIENT EXAMINATION GLOVELYY1989-05-11 View
↑