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FDA 510(k)

RIA KIT, QUANTITOPE CORTISOL

K-Number: K781903 · 1979-01-26

ApplicantKallestad Laboratories, Inc.
Decision Date1979-01-26
Product CodeCGR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

RIA KIT, QUANTITOPE CORTISOL is the device name listed in this FDA 510(k) record. The listed applicant is Kallestad Laboratories, Inc.. It received FDA 510(k) clearance on 1979-01-26 under 510(k) number K781903. 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 RIA KIT, QUANTITOPE CORTISOL?

RIA KIT, QUANTITOPE CORTISOL is a medical device that received FDA 510(k) clearance on 1979-01-26. The listed applicant is Kallestad Laboratories, Inc.. The 510(k) number is K781903.

When did RIA KIT, QUANTITOPE CORTISOL receive FDA 510(k) clearance?

RIA KIT, QUANTITOPE CORTISOL received FDA 510(k) clearance on 1979-01-26, under 510(k) number K781903.

Who is the listed applicant for RIA KIT, QUANTITOPE CORTISOL?

The FDA 510(k) record lists Kallestad Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RIA KIT, QUANTITOPE CORTISOL?

The FDA product code for RIA KIT, QUANTITOPE CORTISOL is CGR.

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Other records listing Kallestad Laboratories, Inc. as applicant

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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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