
Bausch & Lomb, Inc.
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RENU MULTIPLUS MULTI-PURPOSE SOLUTION is an FDA 510(k)-cleared medical device (K990422) 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 April 26, 1999. Regulation: 8.

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