<GENX> SPERM WASHING MEDIA
K-Number: K991022 · 1999-09-09
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Device Summary
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.
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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