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QUANTIMETRIC 2 TEST KIT

K813242 Class I Traditional
Decision Date
1981-12-02
Sponsor / Applicant
Kallestad Laboratories, Inc.

Technical Specification

510(k) Submission ID K813242
Product Code KEW
Medical Specialty / Panel Pathology
Regulation Citation 21 CFR 864.3010
Decision Date 1981-12-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QUANTIMETRIC 2 TEST KIT received FDA 510(k) clearance under submission number K813242, sponsored by Kallestad Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Pathology review panel. The statutory decision date of record is 1981-12-02.

Classification & Regulation

This clearance is catalogued under FDA product code KEW and 21 CFR 864.3010, within the Pathology review panel as a Class I device.