meddevicedb.com FDA Device Reference

E-Z FLO + SET

K902330 Class II Traditional
Decision Date
1990-09-21
Sponsor / Applicant
Prn Services, Inc.

Technical Specification

510(k) Submission ID K902330
Product Code FPA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 1990-09-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

E-Z FLO + SET received FDA 510(k) clearance under submission number K902330, sponsored by Prn Services, 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 1990-09-21.

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.