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FDA 510(k)

Bausch + Lomb Sensitive Eyes Plus Saline Solution

K-Number: K170483 · 2017-04-11

ApplicantBausch & Lomb, Incorporated
Decision Date2017-04-11
Product CodeLPN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

Bausch + Lomb Sensitive Eyes Plus Saline Solution is a medical device manufactured by Bausch & Lomb, Incorporated. It received FDA 510(k) clearance on 2017-04-11 under approval 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. It is manufactured by Bausch & Lomb, Incorporated. The 510(k) number is K170483.

When was Bausch + Lomb Sensitive Eyes Plus Saline Solution approved by the FDA?

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

What company makes Bausch + Lomb Sensitive Eyes Plus Saline Solution?

Bausch + Lomb Sensitive Eyes Plus Saline Solution is manufactured by Bausch & Lomb, Incorporated.

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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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.

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