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.

Preswede AB

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K033933 POWERLITE 600 EX SYSTEMGEX2004-03-16 View
510(k) K030423 POWERLITE 600 EP SYSTEMGEX2003-05-09 View
↑