<GENX> FERTILIZATION MEDIA-HTF
K-Number: K991173 · 1999-07-19
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Device Summary
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.
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
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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