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.

Diomedics, Inc.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K073503 VERSA LITEFTC2008-01-23 View
510(k) K982546 PHASER-2000ILY1998-09-22 View
510(k) K926224 DIOMEDICS SURGI LIGHT/LIGHT TOUCH OPTICAL FIBERSGEX1993-07-22 View
↑