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FDA 510(k)

QUANTIMUNE CORTISOL RIA CORTISOL RADIO-

K-Number: K800045 · 1980-01-23

ApplicantBio-Rad
Decision Date1980-01-23
Product CodeCGR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

QUANTIMUNE CORTISOL RIA CORTISOL RADIO- is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 1980-01-23 under 510(k) number K800045. The device is classified under product code CGR. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUANTIMUNE CORTISOL RIA CORTISOL RADIO-?

QUANTIMUNE CORTISOL RIA CORTISOL RADIO- is a medical device that received FDA 510(k) clearance on 1980-01-23. The listed applicant is Bio-Rad. The 510(k) number is K800045.

When did QUANTIMUNE CORTISOL RIA CORTISOL RADIO- receive FDA 510(k) clearance?

QUANTIMUNE CORTISOL RIA CORTISOL RADIO- received FDA 510(k) clearance on 1980-01-23, under 510(k) number K800045.

Who is the listed applicant for QUANTIMUNE CORTISOL RIA CORTISOL RADIO-?

The FDA 510(k) record lists Bio-Rad as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUANTIMUNE CORTISOL RIA CORTISOL RADIO-?

The FDA product code for QUANTIMUNE CORTISOL RIA CORTISOL RADIO- is CGR.

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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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