FDA 510(k) Applications Submitted by BAUSCH & LOMB, INC

FDA 510(k) Number Submission Date Device Name Applicant
K173480 11/13/2017 Crystalsert Lens Delivery System Bausch & Lomb, Inc
K082132 07/29/2008 BAUSCH & LOMB D4600A AIR EXCHANGE LINE PACK BAUSCH & LOMB, INC


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