meddevicedb.com FDA Device Reference

ELVI MUCAPROTEINS

K792554 Class I Traditional
Decision Date
1980-01-16
Sponsor / Applicant
Volu Sol Medical Industries

Technical Specification

510(k) Submission ID K792554
Product Code JQN
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1505
Decision Date 1980-01-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELVI MUCAPROTEINS received FDA 510(k) clearance under submission number K792554, sponsored by Volu Sol Medical Industries. 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 1980-01-16.

Classification & Regulation

This clearance is catalogued under FDA product code JQN and 21 CFR 862.1505, within the Clinical Chemistry review panel as a Class I device.