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PHILIPS EASY VISION FAMILY WORKSTATION OPTION CARDIRAC SCORING

K002942 Class II Traditional
Decision Date
2000-12-19
Sponsor / Applicant
Philips Medical Systems North America, Inc.

Technical Specification

510(k) Submission ID K002942
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2000-12-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PHILIPS EASY VISION FAMILY WORKSTATION OPTION CARDIRAC SCORING received FDA 510(k) clearance under submission number K002942, sponsored by Philips Medical Systems North America, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2000-12-19.

Classification & Regulation

This clearance is catalogued under FDA product code LLZ and 21 CFR 892.2050, within the Radiology review panel as a Class II device.