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FDA 510(k)

CORTISOL 125-I RADIOIMMUNOASSAY KIT

K-Number: K802969 · 1981-01-02

ApplicantRia Products, Inc.
Decision Date1981-01-02
Product CodeCGR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CORTISOL 125-I RADIOIMMUNOASSAY KIT is the device name listed in this FDA 510(k) record. The listed applicant is Ria Products, Inc.. It received FDA 510(k) clearance on 1981-01-02 under 510(k) number K802969. 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 125-I RADIOIMMUNOASSAY KIT?

CORTISOL 125-I RADIOIMMUNOASSAY KIT is a medical device that received FDA 510(k) clearance on 1981-01-02. The listed applicant is Ria Products, Inc.. The 510(k) number is K802969.

When did CORTISOL 125-I RADIOIMMUNOASSAY KIT receive FDA 510(k) clearance?

CORTISOL 125-I RADIOIMMUNOASSAY KIT received FDA 510(k) clearance on 1981-01-02, under 510(k) number K802969.

Who is the listed applicant for CORTISOL 125-I RADIOIMMUNOASSAY KIT?

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

What is the FDA product code for CORTISOL 125-I RADIOIMMUNOASSAY KIT?

The FDA product code for CORTISOL 125-I RADIOIMMUNOASSAY KIT is CGR.

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Other records listing Ria Products, Inc. as applicant

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K813310NO-HOIL COMBOSTAT II KITK801578COMBOSTAT - NO-BOIL KITK801579VITAMIN B12 - NO-BOIL KITK800710FERRITIRON KIT CAT. #RP-1100K800914NO-BOIL FOLATE KIT #RP-500K781844FERRITIN KIT

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Related Devices (Code: 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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