meddevicedb.com FDA Device Reference

SR1 (FSH) IMMUNOENZYMETRIC ASSAY

K892706 Class I Traditional
Decision Date
1989-06-09
Sponsor / Applicant
Serono-Baker Diagnostics, Inc.

Technical Specification

510(k) Submission ID K892706
Product Code CGJ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1300
Decision Date 1989-06-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SR1 (FSH) IMMUNOENZYMETRIC ASSAY received FDA 510(k) clearance under submission number K892706, sponsored by Serono-Baker Diagnostics, 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 1989-06-09.

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.