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FDA 510(k)

WORKBENCH BY <GENX>

K-Number: K020560 · 2002-06-19

ApplicantGenx Intl., Inc.
Decision Date2002-06-19
Product CodeMQG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

WORKBENCH BY <GENX> is the device name listed in this FDA 510(k) record. The listed applicant is Genx Intl., Inc.. It received FDA 510(k) clearance on 2002-06-19 under 510(k) number K020560. The device is classified under product code MQG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WORKBENCH BY <GENX>?

WORKBENCH BY <GENX> is a medical device that received FDA 510(k) clearance on 2002-06-19. The listed applicant is Genx Intl., Inc.. The 510(k) number is K020560.

When did WORKBENCH BY <GENX> receive FDA 510(k) clearance?

WORKBENCH BY <GENX> received FDA 510(k) clearance on 2002-06-19, under 510(k) number K020560.

Who is the listed applicant for WORKBENCH BY <GENX>?

The FDA 510(k) record lists Genx Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WORKBENCH BY <GENX>?

The FDA product code for WORKBENCH BY <GENX> is MQG.

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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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