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FDA 510(k)

COAT-A-COUNT TESTOSTERONE RIA KIT

K-Number: K813401 · 1981-12-22

Decision Date1981-12-22
Product CodeCDZ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

COAT-A-COUNT TESTOSTERONE RIA KIT is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Products Corp.. It received FDA 510(k) clearance on 1981-12-22 under 510(k) number K813401. 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 COAT-A-COUNT TESTOSTERONE RIA KIT?

COAT-A-COUNT TESTOSTERONE RIA KIT is a medical device that received FDA 510(k) clearance on 1981-12-22. The listed applicant is Diagnostic Products Corp.. The 510(k) number is K813401.

When did COAT-A-COUNT TESTOSTERONE RIA KIT receive FDA 510(k) clearance?

COAT-A-COUNT TESTOSTERONE RIA KIT received FDA 510(k) clearance on 1981-12-22, under 510(k) number K813401.

Who is the listed applicant for COAT-A-COUNT TESTOSTERONE RIA KIT?

The FDA 510(k) record lists Diagnostic Products Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COAT-A-COUNT TESTOSTERONE RIA KIT?

The FDA product code for COAT-A-COUNT TESTOSTERONE RIA 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 Diagnostic Products Corp. 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 321 devices →

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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