← Product Code [LLZ](/submissions/RA/subpart-b%E2%80%94diagnostic-devices/LLZ) · K953911

# PHILIPS EASYVISION (K953911)

_Philips Medical Systems, Inc. · LLZ · Jun 27, 1996 · Radiology · SESE_

**Canonical URL:** https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/LLZ/K953911

## Device Facts

- **Applicant:** Philips Medical Systems, Inc.
- **Product Code:** [LLZ](/submissions/RA/subpart-b%E2%80%94diagnostic-devices/LLZ.md)
- **Decision Date:** Jun 27, 1996
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 892.2050
- **Device Class:** Class 2
- **Review Panel:** Radiology
- **Attributes:** Software as a Medical Device

## Device Story

Optional software package for Philips EasyVision CT/MR workstations; enables CT/MR image matching; used by clinicians to overlay or align CT and MR images; facilitates diagnostic review and treatment planning; improves visualization of anatomical structures by combining modalities.

## Clinical Evidence

No clinical data provided; safety and effectiveness based on past experience with substantially equivalent devices.

## Technological Characteristics

Software package for CT/MR workstations; enables image matching/registration functionality.

## Regulatory Identification

A medical image management and processing system is a device that provides one or more capabilities relating to the review and digital processing of medical images for the purposes of interpretation by a trained practitioner of disease detection, diagnosis, or patient management. The software components may provide advanced or complex image processing functions for image manipulation, enhancement, or quantification that are intended for use in the interpretation and analysis of medical images. Advanced image manipulation functions may include image segmentation, multimodality image registration, or 3D visualization. Complex quantitative functions may include semi-automated measurements or time-series measurements.

## Special Controls

*Classification.* Class II (special controls; voluntary standards—Digital Imaging and Communications in Medicine (DICOM) Std., Joint Photographic Experts Group (JPEG) Std., Society of Motion Picture and Television Engineers (SMPTE) Test Pattern).

## Submission Summary (Full Text)

> This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com.
>
> Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/).

{0}

K953911
JUN 27 1996
PHILIPS

# Philips Medical Systems

P.O. Box 10000, 5680 DA Best, Eindhoven, The Netherlands

Department of Health and Human Services
Center for Devices and Radiological Health
Office of Device Evaluation
Pre-Market Notification section.

Quality Assurance Dpt. XSB/XCB
XB030-950608/RR/wp

1995.05.30

## SUMMARY OF SAFETY AND EFFECTIVENESS INFORMATION

for the optional package:

### CT/MR MATCHING

for use in PHILIPS EasyVision CT/MR workstations

This 510(k) summary of safety and effectiveness information is being submitted in accordance with the requirements of SMDA 1990.
The undersigned certifies that the 510(k) Pre-Market notification for the above referenced products contains adequate information and data to enable CDRH to determine substantial equivalence.

This information and data is summarized as follows:

1. The information for Users contains comprehensive information to insure safe and effective use;
2. Past experience with substantially equivalent predicate devices has shown our device to be safe and effective when used as directed in the Information for Users.

R.W. Kijntjes
Approbation Officer
Quality Assurance dept. XSB / XCB
Philips Medical Systems, Best
The Netherlands.

Philips Medical Systems Nederland B.V.
Veenpluis 6, Best, The Netherlands
Tel: +31 40 79 11 11
Fax: +31 40 76 22 05
Commercial Register Eindhoven no. 60498

---

**Source:** [https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/LLZ/K953911](https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/LLZ/K953911)

**Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. If you're preparing [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/), [get in touch](https://innolitics.com/contact).

**Cite:** Innolitics at https://innolitics.com