meddevicedb.com FDA Device Reference

DOCUMENT THYROID CAL*VER

K992034 Class I Traditional
Decision Date
1999-07-23
Sponsor / Applicant
Casco-Nerl Diagnostics Corporation (Maine)

Technical Specification

510(k) Submission ID K992034
Product Code JJY
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 1999-07-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DOCUMENT THYROID CAL*VER received FDA 510(k) clearance under submission number K992034, sponsored by Casco-Nerl Diagnostics Corporation (Maine). 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 1999-07-23.

Classification & Regulation

This clearance is catalogued under FDA product code JJY and 21 CFR 862.1660, within the Clinical Chemistry review panel as a Class I device.