meddevicedb.com FDA Device Reference

CLP COMPREHENSIVE LIPID CONTROL-HR

K896247 Class I Traditional
Decision Date
1990-01-10
Sponsor / Applicant
Creative Laboratory Products, Inc.

Technical Specification

510(k) Submission ID K896247
Product Code JJY
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 1990-01-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CLP COMPREHENSIVE LIPID CONTROL-HR received FDA 510(k) clearance under submission number K896247, sponsored by Creative Laboratory Products, 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 1990-01-10.

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.