
Bausch & Lomb, Inc.
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RENU MULTIPLUS NO RUB MULTI-PURPOSE SOLUTION is an FDA 510(k)-cleared medical device (K011796) manufactured by Bausch & Lomb, 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 October 31, 2001. Regulation: 8.

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