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.

Microvision, Inc.

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

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K022186 SCLERAL PLUGS, 19 AND 20 GAUGELXP2003-02-26 View
510(k) K023481 MICROVISION SCLERAL BUCKLING COMPONENTSHQX2003-01-08 View
510(k) K982462 FIBER OPTIC ENDOILLUMINATION PROBEFFS1998-09-14 View
↑