meddevicedb.com FDA Device Reference

BD INTROSYTE PRECISION INTRODUCER, BD INTROSYTE AUTOGAURD SHIELDED INTRODUCER

K013304 Class I Traditional
Decision Date
2002-01-02
Sponsor / Applicant
Becton Dickinson Infusion Therapy Systems, Inc.

Technical Specification

510(k) Submission ID K013304
Product Code DBY
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5520
Decision Date 2002-01-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BD INTROSYTE PRECISION INTRODUCER, BD INTROSYTE AUTOGAURD SHIELDED INTRODUCER received FDA 510(k) clearance under submission number K013304, sponsored by Becton Dickinson Infusion Therapy Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2002-01-02.

Classification & Regulation

This clearance is catalogued under FDA product code DBY and 21 CFR 866.5520, within the Immunology review panel as a Class I device.