meddevicedb.com FDA Device Reference

NYLUS PICC

K113225 Class II Traditional
Decision Date
2012-11-06
Sponsor / Applicant
Semprus Biosciences

Technical Specification

510(k) Submission ID K113225
Product Code LJS
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5970
Decision Date 2012-11-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NYLUS PICC received FDA 510(k) clearance under submission number K113225, sponsored by Semprus Biosciences. 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 2012-11-06.

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.