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DSL ESTRADIAL RADIOIMMUNOASSAY (DSL-4400)

K870405 Class I Traditional
Decision Date
1987-06-08
Sponsor / Applicant
Diagnostic Systems Laboratories, Inc.

Technical Specification

510(k) Submission ID K870405
Product Code CHP
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1260
Decision Date 1987-06-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DSL ESTRADIAL RADIOIMMUNOASSAY (DSL-4400) received FDA 510(k) clearance under submission number K870405, sponsored by Diagnostic 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 1987-06-08.

Classification & Regulation

This clearance is catalogued under FDA product code CHP and 21 CFR 862.1260, within the Clinical Chemistry review panel as a Class I device.