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Microvision, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
6
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K022186SCLERAL PLUGS, 19 AND 20 GAUGEFebruary 26, 2003
K023481MICROVISION SCLERAL BUCKLING COMPONENTSJanuary 8, 2003
K982462FIBER OPTIC ENDOILLUMINATION PROBESeptember 14, 1998