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MEDIX BIOTECH PROLACTIN ENZYME IMMUNO. TEST KIT

K873355 Class I Traditional
Decision Date
1987-10-09
Sponsor / Applicant
Medix Biotech, Inc.

Technical Specification

510(k) Submission ID K873355
Product Code CFT
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1625
Decision Date 1987-10-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDIX BIOTECH PROLACTIN ENZYME IMMUNO. TEST KIT received FDA 510(k) clearance under submission number K873355, 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 1987-10-09.

Classification & Regulation

This clearance is catalogued under FDA product code CFT and 21 CFR 862.1625, within the Clinical Chemistry review panel as a Class I device.