meddevicedb.com FDA Device Reference

SCIg60 Infusion System

K240148 Class II Special
Decision Date
2024-02-16
Sponsor / Applicant
Emed Technologies Corporation

Technical Specification

510(k) Submission ID K240148
Product Code PKP
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 2024-02-16
Clearance Pathway Special

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 K240148, sponsored by Emed Technologies Corporation. The device was reviewed via the Special premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2024-02-16.

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.