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.

Argus Photonics Group

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K983543 ACCU-PULSE 1000 CO2 SURGICAL LASER SYSTEMGEX1998-12-16 View
510(k) K971830 ACCU-PULSE CARBON DIOXIDE LASER SYSTEMGEX1997-08-14 View
↑