Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Bausch + Lomb Preservative Free Lubricating and Rewetting Drops

K-Number: K222541 · 2022-12-06

Decision Date2022-12-06
Product CodeLPN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

Bausch + Lomb Preservative Free Lubricating and Rewetting Drops 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 2022-12-06 under 510(k) number K222541. 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 Bausch + Lomb Preservative Free Lubricating and Rewetting Drops?

Bausch + Lomb Preservative Free Lubricating and Rewetting Drops is a medical device that received FDA 510(k) clearance on 2022-12-06. The listed applicant is Bausch & Lomb, Incorporated. The 510(k) number is K222541.

When did Bausch + Lomb Preservative Free Lubricating and Rewetting Drops receive FDA 510(k) clearance?

Bausch + Lomb Preservative Free Lubricating and Rewetting Drops received FDA 510(k) clearance on 2022-12-06, under 510(k) number K222541.

Who is the listed applicant for Bausch + Lomb Preservative Free Lubricating and Rewetting Drops?

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 Bausch + Lomb Preservative Free Lubricating and Rewetting Drops?

The FDA product code for Bausch + Lomb Preservative Free Lubricating and Rewetting Drops is LPN.

Related Clinical Trials

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.

Other records listing Bausch & Lomb, Incorporated 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.

View all 38 devices →

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.

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.