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FDA 510(k)

RENU MULTIPLUS MULTI-PURPOSE SOLUTION

K-Number: K974723 · 1998-03-10

ApplicantBausch & Lomb, Inc.
Decision Date1998-03-10
Product CodeLPN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

RENU MULTIPLUS MULTI-PURPOSE SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Bausch & Lomb, Inc.. It received FDA 510(k) clearance on 1998-03-10 under 510(k) number K974723. The device is classified under product code LPN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RENU MULTIPLUS MULTI-PURPOSE SOLUTION?

RENU MULTIPLUS MULTI-PURPOSE SOLUTION is a medical device that received FDA 510(k) clearance on 1998-03-10. The listed applicant is Bausch & Lomb, Inc.. The 510(k) number is K974723.

When did RENU MULTIPLUS MULTI-PURPOSE SOLUTION receive FDA 510(k) clearance?

RENU MULTIPLUS MULTI-PURPOSE SOLUTION received FDA 510(k) clearance on 1998-03-10, under 510(k) number K974723.

Who is the listed applicant for RENU MULTIPLUS MULTI-PURPOSE SOLUTION?

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

What is the FDA product code for RENU MULTIPLUS MULTI-PURPOSE SOLUTION?

The FDA product code for RENU MULTIPLUS MULTI-PURPOSE SOLUTION is LPN.

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Other records listing Bausch & Lomb, Inc. as applicant

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Related Devices (Code: LPN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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