meddevicedb.com FDA Device Reference

EURO DEFI PADS ADULT; EURO DEFI PADS ADULT RADIOTRANSPARENT: EURO DEFI PADS PEDIATRIC

K103783 Class II Traditional
Decision Date
2011-06-16
Sponsor / Applicant
Fiab Spa

Technical Specification

510(k) Submission ID K103783
Product Code LDD
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5300
Decision Date 2011-06-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EURO DEFI PADS ADULT; EURO DEFI PADS ADULT RADIOTRANSPARENT: EURO DEFI PADS PEDIATRIC received FDA 510(k) clearance under submission number K103783, sponsored by Fiab Spa. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2011-06-16.

Classification & Regulation

This clearance is catalogued under FDA product code LDD and 21 CFR 870.5300, within the Cardiovascular review panel as a Class II device.