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FDA 510(k)

REFRESH CONTACTS LUBRICATING AND REWETTING DROPS

K-Number: K992028 · 1999-10-07

ApplicantAllergan, Inc.
Decision Date1999-10-07
Product CodeLPN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

REFRESH CONTACTS LUBRICATING AND REWETTING DROPS is the device name listed in this FDA 510(k) record. The listed applicant is Allergan, Inc.. It received FDA 510(k) clearance on 1999-10-07 under 510(k) number K992028. 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 REFRESH CONTACTS LUBRICATING AND REWETTING DROPS?

REFRESH CONTACTS LUBRICATING AND REWETTING DROPS is a medical device that received FDA 510(k) clearance on 1999-10-07. The listed applicant is Allergan, Inc.. The 510(k) number is K992028.

When did REFRESH CONTACTS LUBRICATING AND REWETTING DROPS receive FDA 510(k) clearance?

REFRESH CONTACTS LUBRICATING AND REWETTING DROPS received FDA 510(k) clearance on 1999-10-07, under 510(k) number K992028.

Who is the listed applicant for REFRESH CONTACTS LUBRICATING AND REWETTING DROPS?

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

What is the FDA product code for REFRESH CONTACTS LUBRICATING AND REWETTING DROPS?

The FDA product code for REFRESH CONTACTS LUBRICATING AND REWETTING DROPS is LPN.

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Other records listing Allergan, 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.

K190674REFRESH RELIEVA For CONTACTSK161457XEN Glaucoma Treatment SystemK083812REFRESH OPTIVE LENS COMFORT REWETTING DROPSK051852SINGLE AMPLIFIER FOR BOTOXK014202COMPLETE BRAND MULTI-PURPOSE SOLUTIONK013479COMPLETE BRAND MULTI-PURPOSE SOLUTION

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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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