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.

Windwell Agencies Sdn. Bhd.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K894454 PATIENT EXAMINATION GLOVES, LATEXLYY1989-09-26 View
510(k) K892174 LATEX EXAMINATION GLOVES (WINTEX)LYY1989-08-23 View
↑