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FDA 510(k)

CORTISOL REAGENT SYSTEM

K-Number: K760939 · 1976-11-16

ApplicantBeckman Instruments, Inc.
Decision Date1976-11-16
Product CodeCGR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CORTISOL REAGENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Beckman Instruments, Inc.. It received FDA 510(k) clearance on 1976-11-16 under 510(k) number K760939. 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 CORTISOL REAGENT SYSTEM?

CORTISOL REAGENT SYSTEM is a medical device that received FDA 510(k) clearance on 1976-11-16. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K760939.

When did CORTISOL REAGENT SYSTEM receive FDA 510(k) clearance?

CORTISOL REAGENT SYSTEM received FDA 510(k) clearance on 1976-11-16, under 510(k) number K760939.

Who is the listed applicant for CORTISOL REAGENT SYSTEM?

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

What is the FDA product code for CORTISOL REAGENT SYSTEM?

The FDA product code for CORTISOL REAGENT SYSTEM is CGR.

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Other records listing Beckman Instruments, 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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