
Acufex Microsurgical, Inc.
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ACUFEX COMPARATIVE SURGICAL KERATOMETER is an FDA 510(k)-cleared medical device (K852424) manufactured by Acufex Microsurgical, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 10, 1985. Regulation: 8.

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