meddevicedb.com FDA Device Reference

ELECSYS ESTRADIOL CALSET II

K992981 Class II Traditional
Decision Date
1999-09-24
Sponsor / Applicant
Roche Diagnostics Corp.

Technical Specification

510(k) Submission ID K992981
Product Code JIT
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1150
Decision Date 1999-09-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELECSYS ESTRADIOL CALSET II received FDA 510(k) clearance under submission number K992981, sponsored by Roche Diagnostics Corp.. 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 1999-09-24.

Classification & Regulation

This clearance is catalogued under FDA product code JIT and 21 CFR 862.1150, within the Clinical Chemistry review panel as a Class II device.