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AUTOHDL CHOLESTEROL REAGENT SET

K992002 Class I Traditional
Decision Date
1999-08-05
Sponsor / Applicant
Pointe Scientific, Inc.,

Technical Specification

510(k) Submission ID K992002
Product Code LBR
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1475
Decision Date 1999-08-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AUTOHDL CHOLESTEROL REAGENT SET received FDA 510(k) clearance under submission number K992002, sponsored by Pointe Scientific, 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 1999-08-05.

Classification & Regulation

This clearance is catalogued under FDA product code LBR and 21 CFR 862.1475, within the Clinical Chemistry review panel as a Class I device.