meddevicedb.com FDA Device Reference

Sonopet iQ Sterilization Tray

K190667 Class II Traditional
Decision Date
2019-06-13
Sponsor / Applicant
Paragon Medical

Technical Specification

510(k) Submission ID K190667
Product Code KCT
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6850
Decision Date 2019-06-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Sonopet iQ Sterilization Tray received FDA 510(k) clearance under submission number K190667, sponsored by Paragon Medical. 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 2019-06-13.

Classification & Regulation

This clearance is catalogued under FDA product code KCT and 21 CFR 880.6850, within the General Hospital review panel as a Class II device.