meddevicedb.com FDA Device Reference

SCIg60 Infusion System

K222087 Class II Traditional
Decision Date
2022-10-13
Sponsor / Applicant
Emed Technologies Corporation

Technical Specification

510(k) Submission ID K222087
Product Code PKP
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 2022-10-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SCIg60 Infusion System received FDA 510(k) clearance under submission number K222087, sponsored by Emed Technologies Corporation. 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 2022-10-13.

Classification & Regulation

This clearance is catalogued under FDA product code PKP and 21 CFR 880.5725, within the General Hospital review panel as a Class II device.