meddevicedb.com FDA Device Reference

Solana GAS Assay, Solana instrument

K150868 Class II Traditional
Decision Date
2015-06-23
Sponsor / Applicant
Quidel Corporation

Technical Specification

510(k) Submission ID K150868
Product Code PGX
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.2680
Decision Date 2015-06-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Solana GAS Assay, Solana instrument received FDA 510(k) clearance under submission number K150868, sponsored by Quidel Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2015-06-23.

Classification & Regulation

This clearance is catalogued under FDA product code PGX and 21 CFR 866.2680, within the Microbiology review panel as a Class II device.