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FDA 510(k)

RENU MULTIPLUS LUBRICATING & REWETTING DROPS

K-Number: K980591 · 1998-06-24

ApplicantBausch & Lomb, Inc.
Decision Date1998-06-24
Product CodeLPN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

RENU MULTIPLUS LUBRICATING & REWETTING DROPS 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 1998-06-24 under 510(k) number K980591. 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 LUBRICATING & REWETTING DROPS?

RENU MULTIPLUS LUBRICATING & REWETTING DROPS is a medical device that received FDA 510(k) clearance on 1998-06-24. The listed applicant is Bausch & Lomb, Inc.. The 510(k) number is K980591.

When did RENU MULTIPLUS LUBRICATING & REWETTING DROPS receive FDA 510(k) clearance?

RENU MULTIPLUS LUBRICATING & REWETTING DROPS received FDA 510(k) clearance on 1998-06-24, under 510(k) number K980591.

Who is the listed applicant for RENU MULTIPLUS LUBRICATING & REWETTING DROPS?

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 LUBRICATING & REWETTING DROPS?

The FDA product code for RENU MULTIPLUS LUBRICATING & REWETTING DROPS is LPN.

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Other records listing Bausch & Lomb, Inc. as applicant

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.

K192005Bausch + Lomb PreVue Inserter for enVista PreloadedK173480Crystalsert Lens Delivery SystemK161012Easy-Load Lens Delivery SystemK131208BAUSCH + LOMB PROCOMFORT (SAMFILCON A) CONTACT LENS, BAUSCH + LOMB PROCOMFORT (SAMFILCON A) CONTACT LENS FOR PRESBYOPIA,K122575BAUSCH & LOMB PUREVISION (BALAFILCON A) VISIBILITY TINTED CONTACT LENS, BAUSCH & LOMB PUREVISION TORIC (BALAFILCON A) VIK113852BAUSCH & LOMB IOL INJECTOR

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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.

K253795MeniSept 3% Hydrogen Peroxide Cleaning & Disinfecting SolutionMenicon Co, Ltd.K222541Bausch + Lomb Preservative Free Lubricating and Rewetting DropsBausch & Lomb, IncorporatedK221263Aqua Naina Plus Sterile Saline SolutionChemtex USA, Inc.K202932ABT12 multi-purpose solutionBausch & Lomb, IncorporatedK210051OTE MPS 045 Multi-purpose Lens Care SolutionOte North America, LLCK193441Aqua Naina Sterile Saline SolutionChemtex USA, Inc.

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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