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.

Heart Technology, Inc.

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K933238 ROTABLATOR, MODIFICATIONMCW1993-08-24 View
510(k) K914581 HEART TECHNOLOGY WIRECLIPDQX1992-01-06 View
510(k) K913450 HEART TECHNOLOGY ROTABLATOR WIRECLIPMCW1991-09-06 View
510(k) K901206 ROTABLATORMCW1990-09-14 View
↑