Cleared Traditional

K870969 - CORTISOL-RIA KIT COATED TUBE RADIOIMMUNOASSAY KIT
(FDA 510(k) Clearance)

Jun 1987
Decision
104d
Days
Class 2
Risk

K870969 is an FDA 510(k) clearance for the CORTISOL-RIA KIT COATED TUBE RADIOIMMUNOASSAY KIT. This device is classified as a Radioimmunoassay, Cortisol (Class II - Special Controls, product code CGR).

Submitted by Canadian Bioclinical, Ltd. (Ontario Mix 1b4, CA). The FDA issued a Cleared decision on June 22, 1987, 104 days after receiving the submission on March 10, 1987.

This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1205.

Submission Details

510(k) Number K870969 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 10, 1987
Decision Date June 22, 1987
Days to Decision 104 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary

Device Classification

Product Code CGR — Radioimmunoassay, Cortisol
Device Class Class II - Special Controls
CFR Regulation 21 CFR 862.1205

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