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.

Hennig Enterprises Europe Srl

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K020424 V SETFPA2003-08-29 View
510(k) K020421 GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICESMEA2003-04-29 View
↑