meddevicedb.com FDA Device Reference

INTELLIVUE CLINICAL INFORMATION PORTFOLIO

K100272 Class II Special
Decision Date
2010-04-14
Sponsor / Applicant
Philips Medical Systems

Technical Specification

510(k) Submission ID K100272
Product Code DXJ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2450
Decision Date 2010-04-14
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INTELLIVUE CLINICAL INFORMATION PORTFOLIO received FDA 510(k) clearance under submission number K100272, sponsored by Philips Medical Systems. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2010-04-14.

Classification & Regulation

This clearance is catalogued under FDA product code DXJ and 21 CFR 870.2450, within the Cardiovascular review panel as a Class II device.