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FDA 510(k)

CYNOSURE PHOTOGENICA NEO-V

K-Number: K004039 · 2001-03-29

ApplicantCynosure, Inc.
Decision Date2001-03-29
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CYNOSURE PHOTOGENICA NEO-V is the device name listed in this FDA 510(k) record. The listed applicant is Cynosure, Inc.. It received FDA 510(k) clearance on 2001-03-29 under 510(k) number K004039. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CYNOSURE PHOTOGENICA NEO-V?

CYNOSURE PHOTOGENICA NEO-V is a medical device that received FDA 510(k) clearance on 2001-03-29. The listed applicant is Cynosure, Inc.. The 510(k) number is K004039.

When did CYNOSURE PHOTOGENICA NEO-V receive FDA 510(k) clearance?

CYNOSURE PHOTOGENICA NEO-V received FDA 510(k) clearance on 2001-03-29, under 510(k) number K004039.

Who is the listed applicant for CYNOSURE PHOTOGENICA NEO-V?

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 CYNOSURE PHOTOGENICA NEO-V?

The FDA product code for CYNOSURE PHOTOGENICA NEO-V is GEX. This falls under the Gastroenterology category.

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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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