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FDA 510(k)

NNR06 Multi-Purpose Solution

K-Number: K161819 · 2016-11-25

ApplicantBausch & Lomb, Incorporated
Decision Date2016-11-25
Product CodeLPN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

NNR06 Multi-Purpose 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 2016-11-25 under 510(k) number K161819. 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 NNR06 Multi-Purpose Solution?

NNR06 Multi-Purpose Solution is a medical device that received FDA 510(k) clearance on 2016-11-25. The listed applicant is Bausch & Lomb, Incorporated. The 510(k) number is K161819.

When did NNR06 Multi-Purpose Solution receive FDA 510(k) clearance?

NNR06 Multi-Purpose Solution received FDA 510(k) clearance on 2016-11-25, under 510(k) number K161819.

Who is the listed applicant for NNR06 Multi-Purpose 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 NNR06 Multi-Purpose Solution?

The FDA product code for NNR06 Multi-Purpose Solution is LPN.

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Other records listing Bausch & Lomb, Incorporated as applicant

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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.

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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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