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Prescott'S, Inc.
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PRESCOTT'S SURGICAL SPEAR is an FDA 510(k)-cleared medical device (K003842) manufactured by Prescott'S, 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 April 12, 2001. Regulation: 8.