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DSL ACTIVE TESTOSTERONE RIA (DSL #4000)

K854671 Class I Traditional
Decision Date
1985-12-19
Sponsor / Applicant
Diagnostic Systems Laboratories, Inc.

Technical Specification

510(k) Submission ID K854671
Product Code CDZ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1680
Decision Date 1985-12-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DSL ACTIVE TESTOSTERONE RIA (DSL #4000) received FDA 510(k) clearance under submission number K854671, 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 1985-12-19.

Classification & Regulation

This clearance is catalogued under FDA product code CDZ and 21 CFR 862.1680, within the Clinical Chemistry review panel as a Class I device.