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STRATUS HCG FLUOROMETRIC ENZYME IMMUNOASSAY

K850570 Class II Traditional
Decision Date
1985-04-02
Sponsor / Applicant
American Dade

Technical Specification

510(k) Submission ID K850570
Product Code JHI
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1155
Decision Date 1985-04-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STRATUS HCG FLUOROMETRIC ENZYME IMMUNOASSAY received FDA 510(k) clearance under submission number K850570, sponsored by American Dade. 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 1985-04-02.

Classification & Regulation

This clearance is catalogued under FDA product code JHI and 21 CFR 862.1155, within the Clinical Chemistry review panel as a Class II device.