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FDA 510(k)

<GENX> CODA INCUBATOR CELLMATE

K-Number: K001600 · 2000-11-22

Applicant<Genx> Intl., Inc.
Decision Date2000-11-22
Product CodeMQG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

<GENX> CODA INCUBATOR CELLMATE 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 2000-11-22 under 510(k) number K001600. 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 <GENX> CODA INCUBATOR CELLMATE?

<GENX> CODA INCUBATOR CELLMATE is a medical device that received FDA 510(k) clearance on 2000-11-22. The listed applicant is <Genx> Intl., Inc.. The 510(k) number is K001600.

When did <GENX> CODA INCUBATOR CELLMATE receive FDA 510(k) clearance?

<GENX> CODA INCUBATOR CELLMATE received FDA 510(k) clearance on 2000-11-22, under 510(k) number K001600.

Who is the listed applicant for <GENX> CODA INCUBATOR CELLMATE?

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 <GENX> CODA INCUBATOR CELLMATE?

The FDA product code for <GENX> CODA INCUBATOR CELLMATE is MQG.

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Related Devices (Code: 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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