FREE TESTOSTERONE ENZYMEIMMUNOASSAY (EIA) KIT
K-Number: K030730 · 2003-08-18
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Device Summary
Frequently Asked Questions
What is the FREE TESTOSTERONE ENZYMEIMMUNOASSAY (EIA) KIT?
FREE TESTOSTERONE ENZYMEIMMUNOASSAY (EIA) KIT is a medical device that received FDA 510(k) clearance on 2003-08-18. The listed applicant is Diagnostics Biochem Canada, Inc.. The 510(k) number is K030730.
When did FREE TESTOSTERONE ENZYMEIMMUNOASSAY (EIA) KIT receive FDA 510(k) clearance?
FREE TESTOSTERONE ENZYMEIMMUNOASSAY (EIA) KIT received FDA 510(k) clearance on 2003-08-18, under 510(k) number K030730.
Who is the listed applicant for FREE TESTOSTERONE ENZYMEIMMUNOASSAY (EIA) KIT?
The FDA 510(k) record lists Diagnostics Biochem Canada, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FREE TESTOSTERONE ENZYMEIMMUNOASSAY (EIA) KIT?
The FDA product code for FREE TESTOSTERONE ENZYMEIMMUNOASSAY (EIA) KIT is CDZ.
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 Diagnostics Biochem Canada, 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: CDZ)
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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