meddevicedb.com FDA Device Reference

FSH ENZYME IMMUNOASSAY TEST KIT NO. MB-1057

K881596 Class I Traditional
Decision Date
1988-05-27
Sponsor / Applicant
Medix Biotech, Inc.

Technical Specification

510(k) Submission ID K881596
Product Code CGJ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1300
Decision Date 1988-05-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FSH ENZYME IMMUNOASSAY TEST KIT NO. MB-1057 received FDA 510(k) clearance under submission number K881596, 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 1988-05-27.

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.