meddevicedb.com FDA Device Reference

BENT WINGED MINI-VOL INFUSION SET

K842143 Class II Traditional
Decision Date
1984-07-20
Sponsor / Applicant
Med Fusion Systems, Inc.

Technical Specification

510(k) Submission ID K842143
Product Code FPA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 1984-07-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BENT WINGED MINI-VOL INFUSION SET received FDA 510(k) clearance under submission number K842143, sponsored by Med Fusion Systems, 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 1984-07-20.

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.