meddevicedb.com FDA Device Reference

Q2 IV Administration Sets

K213588 Class II Traditional
Decision Date
2022-06-02
Sponsor / Applicant
Quest Medical, Inc.

Technical Specification

510(k) Submission ID K213588
Product Code FPA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 2022-06-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Q2 IV Administration Sets received FDA 510(k) clearance under submission number K213588, sponsored by Quest Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2022-06-02.

Classification & Regulation

This clearance is catalogued under FDA product code FPA and 21 CFR 880.5440, within the General Hospital review panel as a Class II device.