Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

H&A Mui Enterprises, Inc.

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

Total Devices2
Categories2
Latest Approval2023-07-28
TypeNumberDevice NameCodeDate
510(k) K222587 PatCom Distal Chip Endoscope EOB 2023-07-28 View
510(k) K192691 PatCom Single-Use Introducer FED 2020-02-21 View