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FDA 510(k)

LASER FIBER GF500

K-Number: K021686 · 2002-08-20

ApplicantW.O.M. World of Medicine AG
Decision Date2002-08-20
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LASER FIBER GF500 is the device name listed in this FDA 510(k) record. The listed applicant is W.O.M. World of Medicine AG. It received FDA 510(k) clearance on 2002-08-20 under 510(k) number K021686. 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 LASER FIBER GF500?

LASER FIBER GF500 is a medical device that received FDA 510(k) clearance on 2002-08-20. The listed applicant is W.O.M. World of Medicine AG. The 510(k) number is K021686.

When did LASER FIBER GF500 receive FDA 510(k) clearance?

LASER FIBER GF500 received FDA 510(k) clearance on 2002-08-20, under 510(k) number K021686.

Who is the listed applicant for LASER FIBER GF500?

The FDA 510(k) record lists W.O.M. World of Medicine AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LASER FIBER GF500?

The FDA product code for LASER FIBER GF500 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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