Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

FREE TESTOSTERONE ENZYMEIMMUNOASSAY (EIA) KIT

K-Number: K030730 · 2003-08-18

Decision Date2003-08-18
Product CodeCDZ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

FREE TESTOSTERONE ENZYMEIMMUNOASSAY (EIA) KIT is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostics Biochem Canada, Inc.. It received FDA 510(k) clearance on 2003-08-18 under 510(k) number K030730. The device is classified under product code CDZ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

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.

↑