meddevicedb.com FDA Device Reference

SIGMA PROCEDURE 47-UV

K842013 Class II Traditional
Decision Date
1984-06-25
Sponsor / Applicant
Sigma Chemical Co.

Technical Specification

510(k) Submission ID K842013
Product Code CGS
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1215
Decision Date 1984-06-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SIGMA PROCEDURE 47-UV received FDA 510(k) clearance under submission number K842013, sponsored by Sigma Chemical 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 1984-06-25.

Classification & Regulation

This clearance is catalogued under FDA product code CGS and 21 CFR 862.1215, within the Clinical Chemistry review panel as a Class II device.