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FDA 510(k)

LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEM

K-Number: K062930 · 2006-11-08

ApplicantAlcon Research, Ltd.
Decision Date2006-11-08
Product CodeNCF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Alcon Research, Ltd.. It received FDA 510(k) clearance on 2006-11-08 under 510(k) number K062930. The device is classified under product code NCF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEM?

LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEM is a medical device that received FDA 510(k) clearance on 2006-11-08. The listed applicant is Alcon Research, Ltd.. The 510(k) number is K062930.

When did LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEM receive FDA 510(k) clearance?

LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEM received FDA 510(k) clearance on 2006-11-08, under 510(k) number K062930.

Who is the listed applicant for LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEM?

The FDA 510(k) record lists Alcon Research, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEM?

The FDA product code for LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEM is NCF.

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Related Devices (Code: NCF)

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.

K050336OPD-STATION SOFTWARENidek, Inc.K023249ALCON LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEMAlcon Laboratories, Inc.K000637CUSTOMCORNEA MEASUREMENT DEVICE (CCMD)Alcon Laboratories, Inc.

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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