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FDA 510(k)

CYNOSURE ERASURE LASER

K-Number: K984517 · 1999-01-20

ApplicantCynosure, Inc.
Decision Date1999-01-20
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CYNOSURE ERASURE 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 1999-01-20 under 510(k) number K984517. 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 ERASURE LASER?

CYNOSURE ERASURE LASER is a medical device that received FDA 510(k) clearance on 1999-01-20. The listed applicant is Cynosure, Inc.. The 510(k) number is K984517.

When did CYNOSURE ERASURE LASER receive FDA 510(k) clearance?

CYNOSURE ERASURE LASER received FDA 510(k) clearance on 1999-01-20, under 510(k) number K984517.

Who is the listed applicant for CYNOSURE ERASURE 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 ERASURE LASER?

The FDA product code for CYNOSURE ERASURE 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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