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FDA 510(k)

ALCON LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEM

K-Number: K023249 · 2002-10-18

Decision Date2002-10-18
Product CodeNCF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ALCON LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Alcon Laboratories, Inc.. It received FDA 510(k) clearance on 2002-10-18 under 510(k) number K023249. 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 ALCON LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEM?

ALCON LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEM is a medical device that received FDA 510(k) clearance on 2002-10-18. The listed applicant is Alcon Laboratories, Inc.. The 510(k) number is K023249.

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

ALCON LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEM received FDA 510(k) clearance on 2002-10-18, under 510(k) number K023249.

Who is the listed applicant for ALCON LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEM?

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

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

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

Related Clinical Trials

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.

Other records listing Alcon Laboratories, Inc. as applicant

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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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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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