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HYDROXYPROGESTERONE BY RIA 17A

K840886 Class I Traditional
Decision Date
1984-04-18
Sponsor / Applicant
Radioassay Systems Laboratories, Inc.

Technical Specification

510(k) Submission ID K840886
Product Code JLS
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1620
Decision Date 1984-04-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HYDROXYPROGESTERONE BY RIA 17A received FDA 510(k) clearance under submission number K840886, sponsored by Radioassay Systems Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1984-04-18.

Classification & Regulation

This clearance is catalogued under FDA product code JLS and 21 CFR 862.1620, within the Clinical Chemistry review panel as a Class I device.