SPERM WASH MEDIUM WITH GENTAMICIN
K-Number: K023717 · 2002-12-13
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Device Summary
Frequently Asked Questions
What is the SPERM WASH MEDIUM WITH GENTAMICIN?
SPERM WASH MEDIUM WITH GENTAMICIN is a medical device that received FDA 510(k) clearance on 2002-12-13. The listed applicant is Conception Technologies. The 510(k) number is K023717.
When did SPERM WASH MEDIUM WITH GENTAMICIN receive FDA 510(k) clearance?
SPERM WASH MEDIUM WITH GENTAMICIN received FDA 510(k) clearance on 2002-12-13, under 510(k) number K023717.
Who is the listed applicant for SPERM WASH MEDIUM WITH GENTAMICIN?
The FDA 510(k) record lists Conception Technologies as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SPERM WASH MEDIUM WITH GENTAMICIN?
The FDA product code for SPERM WASH MEDIUM WITH GENTAMICIN 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 Conception Technologies 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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