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FLOWPICC CATHETER

K082481 Class II Traditional
Decision Date
2008-12-17
Sponsor / Applicant
Vasonova, Inc.

Technical Specification

510(k) Submission ID K082481
Product Code LJS
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5970
Decision Date 2008-12-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FLOWPICC CATHETER received FDA 510(k) clearance under submission number K082481, sponsored by Vasonova, 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 2008-12-17.

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.