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INTELLISPACE PACS 4.X

K111804 Class II Traditional
Decision Date
2011-07-28
Sponsor / Applicant
Philips Healthcare Informatics, Inc.

Technical Specification

510(k) Submission ID K111804
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2011-07-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INTELLISPACE PACS 4.X received FDA 510(k) clearance under submission number K111804, sponsored by Philips Healthcare Informatics, 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 2011-07-28.

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.