meddevicedb.com FDA Device Reference

FOOTPRINT MEDICAL POLYURETHANE PICC CATHETER

K130507 Class II Special
Decision Date
2013-06-03
Sponsor / Applicant
Footprint Medical, Inc.

Technical Specification

510(k) Submission ID K130507
Product Code LJS
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5970
Decision Date 2013-06-03
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FOOTPRINT MEDICAL POLYURETHANE PICC CATHETER received FDA 510(k) clearance under submission number K130507, sponsored by Footprint Medical, 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 2013-06-03.

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.