meddevicedb.com FDA Device Reference

IVAC 59 SERIES UNIVERSAL SET W/ ANTI-FREE FLOW VAL

K925228 Class II Traditional
Decision Date
1993-07-30
Sponsor / Applicant
Y

Technical Specification

510(k) Submission ID K925228
Product Code FPA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 1993-07-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IVAC 59 SERIES UNIVERSAL SET W/ ANTI-FREE FLOW VAL received FDA 510(k) clearance under submission number K925228, sponsored by Y. 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 1993-07-30.

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.