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.

Hausted, Inc.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K943969 MODEL 578 MOBILE SURGICAL STRETCHERFPO1995-01-25 View
510(k) K945431 MODEL 792 CONVERGE, MODEL 793 VISION 2000FPO1995-01-25 View
↑