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FDA 510(k)

<GENX> FERTILIZATION MEDIA-HTF

K-Number: K991173 · 1999-07-19

Decision Date1999-07-19
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

<GENX> FERTILIZATION MEDIA-HTF 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 1999-07-19 under 510(k) number K991173. 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 <GENX> FERTILIZATION MEDIA-HTF?

<GENX> FERTILIZATION MEDIA-HTF is a medical device that received FDA 510(k) clearance on 1999-07-19. The listed applicant is <Genx> Intl., Inc.. The 510(k) number is K991173.

When did <GENX> FERTILIZATION MEDIA-HTF receive FDA 510(k) clearance?

<GENX> FERTILIZATION MEDIA-HTF received FDA 510(k) clearance on 1999-07-19, under 510(k) number K991173.

Who is the listed applicant for <GENX> FERTILIZATION MEDIA-HTF?

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> FERTILIZATION MEDIA-HTF?

The FDA product code for <GENX> FERTILIZATION MEDIA-HTF is MQL.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing <Genx> Intl., Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 32 devices →

Related Devices (Code: MQL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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