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FDA 510(k)

NEXT GENERATION LASER

K-Number: K062624 · 2007-11-05

ApplicantAlcon Laboratories
Decision Date2007-11-05
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

NEXT GENERATION LASER is the device name listed in this FDA 510(k) record. The listed applicant is Alcon Laboratories. It received FDA 510(k) clearance on 2007-11-05 under 510(k) number K062624. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEXT GENERATION LASER?

NEXT GENERATION LASER is a medical device that received FDA 510(k) clearance on 2007-11-05. The listed applicant is Alcon Laboratories. The 510(k) number is K062624.

When did NEXT GENERATION LASER receive FDA 510(k) clearance?

NEXT GENERATION LASER received FDA 510(k) clearance on 2007-11-05, under 510(k) number K062624.

Who is the listed applicant for NEXT GENERATION LASER?

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

What is the FDA product code for NEXT GENERATION LASER?

The FDA product code for NEXT GENERATION LASER is HQF.

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Other records listing Alcon Laboratories 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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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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