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FDA 510(k)

CYNOSUREA ECLILITE AND ECLILITE U

K-Number: K050080 · 2005-05-05

ApplicantCynosure, Inc.
Decision Date2005-05-05
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CYNOSUREA ECLILITE AND ECLILITE U is the device name listed in this FDA 510(k) record. The listed applicant is Cynosure, Inc.. It received FDA 510(k) clearance on 2005-05-05 under 510(k) number K050080. The device is classified under product code FTC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CYNOSUREA ECLILITE AND ECLILITE U?

CYNOSUREA ECLILITE AND ECLILITE U is a medical device that received FDA 510(k) clearance on 2005-05-05. The listed applicant is Cynosure, Inc.. The 510(k) number is K050080.

When did CYNOSUREA ECLILITE AND ECLILITE U receive FDA 510(k) clearance?

CYNOSUREA ECLILITE AND ECLILITE U received FDA 510(k) clearance on 2005-05-05, under 510(k) number K050080.

Who is the listed applicant for CYNOSUREA ECLILITE AND ECLILITE U?

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

What is the FDA product code for CYNOSUREA ECLILITE AND ECLILITE U?

The FDA product code for CYNOSUREA ECLILITE AND ECLILITE U is FTC.

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Related Devices (Code: FTC)

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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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