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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.
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