meddevicedb.com FDA Device Reference

CAVRO IQ-190 SAMPLE PROCESSOR

K822208 Class I Traditional
Decision Date
1982-08-27
Sponsor / Applicant
Cavro Scientific Instruments, Inc.

Technical Specification

510(k) Submission ID K822208
Product Code JQW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2750
Decision Date 1982-08-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CAVRO IQ-190 SAMPLE PROCESSOR received FDA 510(k) clearance under submission number K822208, sponsored by Cavro Scientific Instruments, 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 1982-08-27.

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.