meddevicedb.com FDA Device Reference

QST TM SAMPLE PROCESSOR

K831273 Class I Traditional
Decision Date
1983-06-02
Sponsor / Applicant
Syva Co.

Technical Specification

510(k) Submission ID K831273
Product Code JQW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2750
Decision Date 1983-06-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QST TM SAMPLE PROCESSOR received FDA 510(k) clearance under submission number K831273, sponsored by Syva Co.. 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 1983-06-02.

Classification & Regulation

This clearance is catalogued under FDA product code JQW and 21 CFR 862.2750, within the Clinical Chemistry review panel as a Class I device.