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AVI MODEL 4225 VENTED PIGGYBACK IV ADMIN SET

K912069 Class II Traditional
Decision Date
1993-10-14
Sponsor / Applicant
3M Avi, Inc.

Technical Specification

510(k) Submission ID K912069
Product Code FPA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 1993-10-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AVI MODEL 4225 VENTED PIGGYBACK IV ADMIN SET received FDA 510(k) clearance under submission number K912069, sponsored by 3M Avi, 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 1993-10-14.

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.