FDA 510(k)

Bausch + Lomb Sensitive Eyes Plus Saline Solution

K-Number: K170483 · 2017-04-11

Decision Date2017-04-11

Product CodeLPN

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

Bausch + Lomb Sensitive Eyes Plus Saline 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 2017-04-11 under 510(k) number K170483. 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 Sensitive Eyes Plus Saline Solution?

Bausch + Lomb Sensitive Eyes Plus Saline Solution is a medical device that received FDA 510(k) clearance on 2017-04-11. The listed applicant is Bausch & Lomb, Incorporated. The 510(k) number is K170483.

When did Bausch + Lomb Sensitive Eyes Plus Saline Solution receive FDA 510(k) clearance?

Bausch + Lomb Sensitive Eyes Plus Saline Solution received FDA 510(k) clearance on 2017-04-11, under 510(k) number K170483.

Who is the listed applicant for Bausch + Lomb Sensitive Eyes Plus Saline 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 Bausch + Lomb Sensitive Eyes Plus Saline Solution?

The FDA product code for Bausch + Lomb Sensitive Eyes Plus Saline Solution is LPN.

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Other records listing Bausch & Lomb, Incorporated as applicant

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Related Devices (Code: LPN)

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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.