
Microvision, Inc.
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MICROVISION SCLERAL BUCKLING COMPONENTS is an FDA 510(k)-cleared medical device (K023481) manufactured by Microvision, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 7, 2003. Regulation: 8.