meddevicedb.com FDA Device Reference

PICC (CT RATED AND NON-RATED)

K083873 Class II Traditional
Decision Date
2009-03-19
Sponsor / Applicant
Pfm Medical, Inc.

Technical Specification

510(k) Submission ID K083873
Product Code LJS
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5970
Decision Date 2009-03-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PICC (CT RATED AND NON-RATED) received FDA 510(k) clearance under submission number K083873, sponsored by Pfm Medical, 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 2009-03-19.

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.