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PARAMAX MAGNESIUM REAGENT

K840784 Class I Traditional
Decision Date
1984-04-13
Sponsor / Applicant
American Dade

Technical Specification

510(k) Submission ID K840784
Product Code JGJ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1495
Decision Date 1984-04-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PARAMAX MAGNESIUM REAGENT received FDA 510(k) clearance under submission number K840784, 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 1984-04-13.

Classification & Regulation

This clearance is catalogued under FDA product code JGJ and 21 CFR 862.1495, within the Clinical Chemistry review panel as a Class I device.