meddevicedb.com FDA Device Reference

UBI MAGIWEL(TM) FSH QUANTITATIVE

K864080 Class I Traditional
Decision Date
1986-11-13
Sponsor / Applicant
United Biotech, Inc.

Technical Specification

510(k) Submission ID K864080
Product Code CGJ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1300
Decision Date 1986-11-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UBI MAGIWEL(TM) FSH QUANTITATIVE received FDA 510(k) clearance under submission number K864080, sponsored by United 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 1986-11-13.

Classification & Regulation

This clearance is catalogued under FDA product code CGJ and 21 CFR 862.1300, within the Clinical Chemistry review panel as a Class I device.