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FDA 510(k)

CYBERCASES BY BAUSCH & LOMB

K-Number: K013232 · 2001-11-20

ApplicantBausch & Lomb, Inc.
Decision Date2001-11-20
Product CodeLRX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CYBERCASES BY BAUSCH & LOMB is the device name listed in this FDA 510(k) record. The listed applicant is Bausch & Lomb, Inc.. It received FDA 510(k) clearance on 2001-11-20 under 510(k) number K013232. The device is classified under product code LRX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CYBERCASES BY BAUSCH & LOMB?

CYBERCASES BY BAUSCH & LOMB is a medical device that received FDA 510(k) clearance on 2001-11-20. The listed applicant is Bausch & Lomb, Inc.. The 510(k) number is K013232.

When did CYBERCASES BY BAUSCH & LOMB receive FDA 510(k) clearance?

CYBERCASES BY BAUSCH & LOMB received FDA 510(k) clearance on 2001-11-20, under 510(k) number K013232.

Who is the listed applicant for CYBERCASES BY BAUSCH & LOMB?

The FDA 510(k) record lists Bausch & Lomb, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CYBERCASES BY BAUSCH & LOMB?

The FDA product code for CYBERCASES BY BAUSCH & LOMB is LRX.

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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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