FDA 510(k)

Bausch + Lomb Boston Original Cleaner, Bausch + Lomb Boston Original Conditioning Solutions

K-Number: K173089 · 2017-11-27

Decision Date2017-11-27

Product CodeMRC

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

Bausch + Lomb Boston Original Cleaner, Bausch + Lomb Boston Original Conditioning Solutions 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 2017-11-27 under 510(k) number K173089. The device is classified under product code MRC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Bausch + Lomb Boston Original Cleaner, Bausch + Lomb Boston Original Conditioning Solutions?

Bausch + Lomb Boston Original Cleaner, Bausch + Lomb Boston Original Conditioning Solutions is a medical device that received FDA 510(k) clearance on 2017-11-27. The listed applicant is Bausch & Lomb, Incorporated. The 510(k) number is K173089.

When did Bausch + Lomb Boston Original Cleaner, Bausch + Lomb Boston Original Conditioning Solutions receive FDA 510(k) clearance?

Bausch + Lomb Boston Original Cleaner, Bausch + Lomb Boston Original Conditioning Solutions received FDA 510(k) clearance on 2017-11-27, under 510(k) number K173089.

Who is the listed applicant for Bausch + Lomb Boston Original Cleaner, Bausch + Lomb Boston Original Conditioning Solutions?

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 Boston Original Cleaner, Bausch + Lomb Boston Original Conditioning Solutions?

The FDA product code for Bausch + Lomb Boston Original Cleaner, Bausch + Lomb Boston Original Conditioning Solutions is MRC.

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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.