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FDA 510(k)

CYNOSURE CO3 ER:YAG LASER

K-Number: K983034 · 1998-09-10

ApplicantCynosure, Inc.
Decision Date1998-09-10
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CYNOSURE CO3 ER:YAG LASER is the device name listed in this FDA 510(k) record. The listed applicant is Cynosure, Inc.. It received FDA 510(k) clearance on 1998-09-10 under 510(k) number K983034. 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 CO3 ER:YAG LASER?

CYNOSURE CO3 ER:YAG LASER is a medical device that received FDA 510(k) clearance on 1998-09-10. The listed applicant is Cynosure, Inc.. The 510(k) number is K983034.

When did CYNOSURE CO3 ER:YAG LASER receive FDA 510(k) clearance?

CYNOSURE CO3 ER:YAG LASER received FDA 510(k) clearance on 1998-09-10, under 510(k) number K983034.

Who is the listed applicant for CYNOSURE CO3 ER:YAG LASER?

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 CO3 ER:YAG LASER?

The FDA product code for CYNOSURE CO3 ER:YAG LASER 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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