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FDA 510(k)

RENUT MULTIPLUS MULLTI-PURPOSE SOLUTION

K-Number: K020802 · 2002-05-31

ApplicantBausch & Lomb, Incorporated
Decision Date2002-05-31
Product CodeLYL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

RENUT MULTIPLUS MULLTI-PURPOSE SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Bausch & Lomb, Incorporated. It received FDA 510(k) clearance on 2002-05-31 under 510(k) number K020802. The device is classified under product code LYL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RENUT MULTIPLUS MULLTI-PURPOSE SOLUTION?

RENUT MULTIPLUS MULLTI-PURPOSE SOLUTION is a medical device that received FDA 510(k) clearance on 2002-05-31. The listed applicant is Bausch & Lomb, Incorporated. The 510(k) number is K020802.

When did RENUT MULTIPLUS MULLTI-PURPOSE SOLUTION receive FDA 510(k) clearance?

RENUT MULTIPLUS MULLTI-PURPOSE SOLUTION received FDA 510(k) clearance on 2002-05-31, under 510(k) number K020802.

Who is the listed applicant for RENUT MULTIPLUS MULLTI-PURPOSE SOLUTION?

The FDA 510(k) record lists Bausch & Lomb, Incorporated as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RENUT MULTIPLUS MULLTI-PURPOSE SOLUTION?

The FDA product code for RENUT MULTIPLUS MULLTI-PURPOSE SOLUTION is LYL.

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Related Devices (Code: LYL)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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