meddevicedb.com FDA Device Reference

LEAD CONTROL (WHOLE BLOOD) LEVELS 1,2,3,4

K970778 Class I Traditional
Decision Date
1997-04-17
Sponsor / Applicant
More Diagnostics

Technical Specification

510(k) Submission ID K970778
Product Code JJX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 1997-04-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LEAD CONTROL (WHOLE BLOOD) LEVELS 1,2,3,4 received FDA 510(k) clearance under submission number K970778, sponsored by More Diagnostics. 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 1997-04-17.

Classification & Regulation

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