meddevicedb.com FDA Device Reference

CG+ Arrow PICC powered by Arrow VPS Stylet PLUS and Arrow VPS Stylet PLUS

K153487 Class II Special
Decision Date
2016-02-04
Sponsor / Applicant
Arrow International, Inc. (Subsidiary of Teleflex, Inc.)

Technical Specification

510(k) Submission ID K153487
Product Code LJS
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5970
Decision Date 2016-02-04
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CG+ Arrow PICC powered by Arrow VPS Stylet PLUS and Arrow VPS Stylet PLUS received FDA 510(k) clearance under submission number K153487, sponsored by Arrow International, Inc. (Subsidiary of Teleflex, Inc.). The device was reviewed via the Special premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2016-02-04.

Classification & Regulation

This clearance is catalogued under FDA product code LJS and 21 CFR 880.5970, within the General Hospital review panel as a Class II device.