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.

K & G Healthcare Ind., Inc.

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

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K812573 SPIROMETER FILTERCAH1981-10-23 View
510(k) K812139 VACUUM SUCTION FILTERKDQ1981-08-20 View
510(k) K811546 NICHOLAS II, VIRAL-BACTERIAL FILTERCAH1981-08-03 View
↑