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MEDIX VISUAL HCG - M HCG ENZYME IMMUNOASSAY

K860490 Class II Traditional
Decision Date
1986-03-05
Sponsor / Applicant
Medix Biotech, Inc.

Technical Specification

510(k) Submission ID K860490
Product Code JHI
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1155
Decision Date 1986-03-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDIX VISUAL HCG - M HCG ENZYME IMMUNOASSAY received FDA 510(k) clearance under submission number K860490, sponsored by Medix Biotech, 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 1986-03-05.

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.