meddevicedb.com FDA Device Reference

STRATO/INFUSAID DUALPORT VASCULAR ACC. SYSTEM

K951872 Class II Traditional
Decision Date
1995-05-18
Sponsor / Applicant
Strato/Infusaid, Inc.

Technical Specification

510(k) Submission ID K951872
Product Code LJT
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5965
Decision Date 1995-05-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STRATO/INFUSAID DUALPORT VASCULAR ACC. SYSTEM received FDA 510(k) clearance under submission number K951872, sponsored by Strato/Infusaid, 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 1995-05-18.

Classification & Regulation

This clearance is catalogued under FDA product code LJT and 21 CFR 880.5965, within the General Hospital review panel as a Class II device.