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.

Sumirubber Industries (Kedah) Sdn. Bhd.

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

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K984309 NBR 4 MILS, NITRILE EXAMINATION GLOVE NON-STERILE POWDEREDLZA1999-02-12 View
510(k) K984311 NBR4 MILS NITRILE POWDER FREE EXAMINATION GLOVES NON-STERILELZA1999-02-09 View
510(k) K890393 EXAMINATION GLOVESLYY1989-08-10 View
↑