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FDA 510(k)

MEDIA CULTURE SYSTEM

K-Number: K040530 · 2004-06-25

Applicant<Genx> Intl., Inc.
Decision Date2004-06-25
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MEDIA CULTURE SYSTEM 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 2004-06-25 under 510(k) number K040530. The device is classified under product code MQL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDIA CULTURE SYSTEM?

MEDIA CULTURE SYSTEM is a medical device that received FDA 510(k) clearance on 2004-06-25. The listed applicant is <Genx> Intl., Inc.. The 510(k) number is K040530.

When did MEDIA CULTURE SYSTEM receive FDA 510(k) clearance?

MEDIA CULTURE SYSTEM received FDA 510(k) clearance on 2004-06-25, under 510(k) number K040530.

Who is the listed applicant for MEDIA CULTURE SYSTEM?

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 MEDIA CULTURE SYSTEM?

The FDA product code for MEDIA CULTURE SYSTEM is MQL.

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Related Devices (Code: MQL)

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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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