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HUMAN GROWTH HORMONE ENZYME IMMUNOASSAY MB-1015

K896643 Class I Traditional
Decision Date
1989-12-29
Sponsor / Applicant
Medix Biotech, Inc.

Technical Specification

510(k) Submission ID K896643
Product Code CFL
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1370
Decision Date 1989-12-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HUMAN GROWTH HORMONE ENZYME IMMUNOASSAY MB-1015 received FDA 510(k) clearance under submission number K896643, 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 1989-12-29.

Classification & Regulation

This clearance is catalogued under FDA product code CFL and 21 CFR 862.1370, within the Clinical Chemistry review panel as a Class I device.