FDA 510(k) Applications Submitted by MICROVISION, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K022186 07/05/2002 SCLERAL PLUGS, 19 AND 20 GAUGE MICROVISION, INC.
K982462 07/15/1998 FIBER OPTIC ENDOILLUMINATION PROBE MICROVISION, INC.
K023481 10/17/2002 MICROVISION SCLERAL BUCKLING COMPONENTS MICROVISION, INC.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact