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FDA 510(k)

<GENX> SPERM WASHING MEDIA

K-Number: K991022 · 1999-09-09

Decision Date1999-09-09
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

<GENX> SPERM WASHING MEDIA 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 1999-09-09 under 510(k) number K991022. 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> SPERM WASHING MEDIA?

<GENX> SPERM WASHING MEDIA is a medical device that received FDA 510(k) clearance on 1999-09-09. The listed applicant is <Genx> Intl., Inc.. The 510(k) number is K991022.

When did <GENX> SPERM WASHING MEDIA receive FDA 510(k) clearance?

<GENX> SPERM WASHING MEDIA received FDA 510(k) clearance on 1999-09-09, under 510(k) number K991022.

Who is the listed applicant for <GENX> SPERM WASHING MEDIA?

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> SPERM WASHING MEDIA?

The FDA product code for <GENX> SPERM WASHING MEDIA 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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