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FDA 510(k)

CANDELA FAMILY OF PULSE DYE LASER SYSTEMS

K-Number: K050673 · 2005-06-13

ApplicantCandela Corp.
Decision Date2005-06-13
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CANDELA FAMILY OF PULSE DYE LASER SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Candela Corp.. It received FDA 510(k) clearance on 2005-06-13 under 510(k) number K050673. 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 CANDELA FAMILY OF PULSE DYE LASER SYSTEMS?

CANDELA FAMILY OF PULSE DYE LASER SYSTEMS is a medical device that received FDA 510(k) clearance on 2005-06-13. The listed applicant is Candela Corp.. The 510(k) number is K050673.

When did CANDELA FAMILY OF PULSE DYE LASER SYSTEMS receive FDA 510(k) clearance?

CANDELA FAMILY OF PULSE DYE LASER SYSTEMS received FDA 510(k) clearance on 2005-06-13, under 510(k) number K050673.

Who is the listed applicant for CANDELA FAMILY OF PULSE DYE LASER SYSTEMS?

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

What is the FDA product code for CANDELA FAMILY OF PULSE DYE LASER SYSTEMS?

The FDA product code for CANDELA FAMILY OF PULSE DYE LASER SYSTEMS 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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