DATEX-OHMEDA S/5 NETWORK AND CENTRAL '01

K013246 · Datex-Ohmeda · MSX · Dec 11, 2001 · Cardiovascular

Device Facts

• Record ID: K013246
• Device Name: DATEX-OHMEDA S/5 NETWORK AND CENTRAL '01
• Applicant: Datex-Ohmeda
• Product Code: MSX · Cardiovascular
• Decision Date: Dec 11, 2001
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 870.2300
• Device Class: Class 2

Indications for Use

The Datex-Ohmeda S/5 Network and Central is intended to be used with Datex-Ohmeda devices for displaying, storing, printing and otherwise processing information received from other networked devices. The Datex-Ohmeda S/5TM Network and Central transfers information between networked Datex-Ohmeda devices in the Datex-Ohmeda monitor network. It also allows information transfer between several Centrals. Within one Datex-Ohmeda monitor network it allows a networked device to display, store, print and otherwise process information received from other networked devices. The Datex-Ohmeda S/5TM Central maintains the network connections between the Datex-Ohmeda bedside monitors and other networked devices in Datex-Ohmeda monitor network. Furthermore, it coordinates the transfer of information between devices in the Datex-Ohmeda S/5TM Network as well as between the Datex-Ohmeda Network and Hospital Information Systems (HIS). The Datex-Ohmeda S/5TM Central can be used for remote monitor management, storing, printing, viewing or otherwise processing of information from several bedside monitors or other networked devices. The Datex-Ohmeda S/5TM ViewStation can be used for remote monitor management, printing, viewing or otherwise processing of information from several bedside monitors or other networked devices. The Datex-Ohmeda S/5TM Network will be used for patients in the hospital and it is meant for continuous use. The device is for use by qualified personnel only.

Device Story

System consists of networked Datex-Ohmeda monitors and networking hardware (cabling, repeaters). Central station acts as primary communication maintainer; enables real-time display of waveforms, numeric values, and alarms from bedside monitors. Supports anesthesia record keeping, data management, and transfer to Hospital Information Systems (HIS). Features include remote alarm silencing, alarm limit adjustment, and monitor disconnection warnings. ViewStation provides remote display/printing without data storage. Operated by qualified hospital personnel in clinical settings. Enhances patient care via centralized monitoring, data continuity during patient transport, and integrated reporting.

Clinical Evidence

Bench testing only. Compliance with safety and performance standards including EN60950 (electrical safety), EN55022 (EMC), EN1441 (risk analysis), EN475/ISO9703 (alarm signals), and IEEE 802.3 (networking). No clinical data presented.

Technological Characteristics

Networked system using commercial PC hardware, standard graphics controllers, and PC keyboards. Connectivity via IEEE 802.3 Ethernet standards. Supports real-time data transmission, storage, and printing. Software-based central monitoring and remote management. Complies with IEC 60601-1-4 for software safety.

Indications for Use

Indicated for hospital patients requiring continuous physiological monitoring. For use by qualified clinical personnel only.

Regulatory Classification

Identification

A cardiac monitor (including cardiotachometer and rate alarm) is a device used to measure the heart rate from an analog signal produced by an electrocardiograph, vectorcardiograph, or blood pressure monitor. This device may sound an alarm when the heart rate falls outside preset upper and lower limits.

Predicate Devices

• Datex-Ohmeda S/5 Network and Central and Information Center (K000647)

Submission Summary (Full Text)

{0}------------------------------------------------

DEC 1 1 2001

Image /page/0/Picture/1 description: The image is a black and white logo. The logo consists of a large circle with a white letter "D" inside. There is a small square in the upper right corner of the circle.

# Premarket Notification 510(k) Summary As required by section 807.92 Datex-Ohmeda S/5 Network and Central '01

### GENERAL COMPANY INFORMATION as required by 807.92(a)(1)

### COMPANY NAME/ADDRESS/PHONE/FAX:

Datex-Ohmeda 86 Pilgrim Road Needham, MA 02492 USA Tel: [phone] Fax: [phone]

# NAME OF CONTACT:

Mr. Joel Kent

## DATE:

September 25, 2001

### DEVICE NAME as required by 807.92(a)(2)

### TRADE NAME:

Datex-Ohmeda S/5 Network and Central '01

## COMMON NAME:

Clinical network and central station

## CLASSIFICATION NAME:

The following Class III classification appears applicable:

System, network and communication, physiological monitors 870.2910

## NAME OF LEGALLY MARKETED DEVICE FOR WHICH A CLAIM OF SUBSTANTIAL EQUIVALENCE IS MADE as required by 807.92(a)(3)

The Datex-Ohmeda S/5 Network and Central '01 is substantially equivalent in safety and effectiveness to the legally marketed (predicate) Datex-Ohmeda S/5 Network and Central and Information Center (510(k) number: K000647).

K013246 Page 1 of 5

{1}------------------------------------------------

### DEVICE DESCRIPTION as required by 807.92(a)(4)

The Datex-Ohmeda S/5 Network (also referred as D-O Network in the related documentation) is a system, which consists of networked devices (which have separate 510k clearance) and the actual networking hardware. The networked devices are Datex-Ohmeda products containing a network adapter for physical access to the D-O Network as well as software modules supporting network access.

Examples of currently available networked devices are:

1. Datex-Ohmeda S/5 Anesthesia Monitor

2. Datex-Ohmeda S/5 Compact Anesthesia Monitor

3. Datex-Ohmeda S/5 Critical Care Monitor

4. Datex-Ohmeda S/5 Compact Critical Care Monitor

5. Datex-Ohmeda S/5 Light Monitor

6. Datex-Ohmeda S/5 Cardiocap 5 Monitor

7. Datex-Ohmeda S/5 Network and Central, included in this 510(k)

8. Datex-Ohmeda S/5 Telemetry System

The DeioRecorder for Anesthesia (formerly named as Datex-Ohmeda AS/3 Record Keeper.) is also related to the D-O Network as an application using the services provided by the D-O Network.

No changes must be made to the Datex-Ohmeda S/5 Network and Central itself due to a new type of networked device.

The Datex-Ohmeda S/5 Central (also referred to as D-O Central in the related documentation) is the primary maintainer of communication between other networked devices and is, thus, an essential part of the network. The structure and functionality of the revised network corresponds to the structure and functionality of the substantially equivalent predicate device Datex-Ohmeda Network and Central (510(k) number: K000647).

The Datex-Ohmeda Network will be used for real-time communication between devices, for record keeping and for data management in a hospital. Practical examples of currently available features are:

O Transmission and display of measured values and alarms in the Datex-Ohmeda S/5 Central screen (central monitoring) and on the screen of another networked monitor (monitor-to-monitor communication).

O Anesthesia record keeping.

[ Storing and transferring of trend and record keeping data in the network. When the patient is moved from one monitor to another, the data can be transferred with the patient. This feature includes also transferring data from/to an external system (HIS, laboratory, etc.) to/from Datex-Ohmeda S/5 Network.

D Printing of anesthesia records, ICU reports, trend printouts, spirometry loop printouts, waveform snapshot printouts, etc.

The actual networking hardware consists of cabling, patch panels, racks, connectors, repeaters, etc. The networking hardware is similar to the networking hardware of the substantially equivalent predicate device Datex-Ohmeda Network and Central (510(k) number: K000647).

The Datex-Ohmeda S/5 ViewStation is a D-0 Central version that can show real-time curves and numeric information from any monitor residing in the Datex-Ohmeda Network. It also allows printing to laser printer or recording to a strip-chart recorder. The Datex-Ohmeda S/5 ViewStation does not store patient data, or provide any other network services

{2}------------------------------------------------

than display and printing services. The ViewStation uses the same hardware and a subset of the software used by the main Central.

The Datex-Ohmeda S/5 Telemetry System Network is a computer-based system for monitoring patients using telemetry. It consists of a PC based Central Station including moments patients assurence as and up to 16 telemetry transmitters per station. The central station supports arrhythmia monitoring, and measuring and trending of ST changes. An Station Jupports arres has been developed to enable connection of Telemetry central to D-O STS TeleNot I ackage enables transfer of ECG waveforms, ECG related parameters and archythmia information to the D-O Network. Also bed-to-bed services from telemetry sessions to bedside monitors are made available.

The new version of Datex-Ohmeda S/5 Network and Central adds the following features: Commercial hardware: The display driver is a commercial board instead of D-O proprietary boards. The proprietary keyboard is not used anymore, instead there is a commercial keyboard with dedicated "EasyAccess" keys

O User Interface is now mouse controlled in addition to keyboard controlled O Numerical and graphical trends have been added

O Alarm management functionality has been extended: remotely silencing of bedside alarms and changing alarm limits from Datex-Ohmeda S/5 Central or ViewStation have been added

□ Monitor disconnection warning on Central has been added

□ Possibility to start a network recorder from a bedside monitor has been added D TeleNet Package to enable connection of Datex-Ohmeda S/5 Telemetry System to D-O

Network

### INTENDED USE as required by 807.92(a)(5)

The Datex-Ohmeda S/5 Network and Central is intended to be used with Datex-Ohmeda devices for displaying, storing, printing and otherwise processing information received from other networked devices.

The Datex-Ohmeda S/5TM Network and Central transfers information between networked Datex-Ohmeda devices in the Datex-Ohmeda monitor network. It also allows information transfer between several Centrals. Within one Datex-Ohmeda monitor network it allows a networked device to display, store, print and otherwise process information received from other networked devices.

The Datex-Ohmeda S/5TM Central maintains the network connections between the Datex-Ohmeda bedside monitors and other networked devices in Datex-Ohmeda monitor network. Furthermore, it coordinates the transfer of information between devices in the Datex-Ohmeda S/5TM Network as well as between the Datex-Ohmeda Network and Hospital Information Systems (HIS).

The Datex-Ohmeda S/5TM Central can be used for remote monitor management, storing, printing, viewing or otherwise processing of information from several bedside monitors or other networked devices.

The Datex-Ohmeda S/5TM ViewStation can be used for remote monitor management, printing, viewing or otherwise processing of information from several bedside monitors or other networked devices.

The Datex-Ohmeda S/5TM Network will be used for patients in the hospital and it is meant for continuous use.

The device is for use by qualified personnel only.

{3}------------------------------------------------

### SUMMARY OF TECHNOLOGICAL CHARACTERITICS OF DEVICE COMPARED TO THE PREDICATE DEVICE as required by 807.92(a)(6)

The Datex-Ohmeda S/5 Network and Central is substantially equivalent in safety and effectiveness to the Datex-Ohmeda S/5 Network and Central and Information Center (510(k) number: K000647).

Similarities:

The indications for use is the same as in predicate except that "remote monitor management" has been expressed in the statement.

The structure and functionality of the Datex-Ohmeda S/5 Network and Central '01 closely corresponds to the structure and functionality of the Datex-Ohmeda Network and Central '99 (predicate). The basic architecture of Datex- Ohmeda S/5 Network and Central '01 is the same as that of Datex-Ohmeda Network and Central '99 (predicate).

The user interface uses the same basic functionality: Single patient view and multiple patient views are similar to the predicate. Alarm indications are similar.

The ability to have audible alarm indications only on the Central is similar to the predicate.

Differences:

The hardware platform now uses commercial graphics controller and normal PC keyboard instead of D-O proprietary versions.

The user interface can now also be controlled with a mouse. The Central uses a PC keyboard that has labeled special "Easy Access" keys. The earlier keyboard was proprietary with special keys.

Remote monitor management adds the option to silence bedside monitor alarms from the Central and to adjust monitor alarm limits. These functions are by default disabled. They can be activated by the system administrator and activation is password protected.

Numerical and graphical trend display has been added to the Central.

Monitor disconnection warning has been added since Central may in some cases be used for monitoring alarms.

Possibility to start a network recorder from monitor has been added to support work methods of e.g. some intensive care units.

A SW package to enable S/5 Telemetry system integration to the D-O Network has been developed. It uses similar connection to the network as the Central.

Summary:

In summary, the new Datex-Ohmeda S/5 Network and Central, described in this submission is substantially equivalent to the predicate (K000647) device.

{4}------------------------------------------------

# SUMMARY OF NONCLINICAL TESTING FOR THE DEVICE and CONCLUSIONS as required by 807.92(b)(1)(3)

The Datex-Ohmeda S/5 Network and Central '01 complies with the safety standards below and is therefore safe and effective for the intended use. The device has been thoroughly and is therefore safe and orietr. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . environmental tolerance, software validation and verification of specifications. environmental toloration, solling following mandatory and voluntary standards has been made:

- EN60950: 1995 (IEC950 2nd edition) Safety of information technology equipment, 그 including electrical business equipment
- EN 55022: 1994 (IEC-CISPR 22) -- Information technology equipment Radio 내 disturbance characteristics. Limits and methods of measurement
- distance characteristics is not 2011-3, IEC 801-4) -- Electromagnetic compatibility -. Generic immunity standard
- EN 1441, Medical devices Risk analysis l
- EN 475, Medical devices Electrically-generated alarm signals l
- ISO 9703-1, ISO 9703-2, Anesthesia and respiratory care alarm signals l
- . IEC 60601-1-4
- CAN/CSA-C22.2 No 950: Information Technology Equipment Including Electrical 미 Business Equipment
- UL1950: Information Technology Equipment Including Electrical Business Equipment 1
- ISO/IEC 8802-3 (ANSI/IEEE 802.3), EIA/TIA-568, EIA/TIA-TSB40, international 내 network cabling standards

### Conclusion:

- The summary above shows that there are no new questions of safety and effectiveness for the Datex-Ohmeda S/5 Network and Central as compared to the predicate device.

{5}------------------------------------------------

Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850

: 上一篇

DEC 1 1 2001

Mr. Joel C. Kent Manager, Quality and Regulatory Affairs Datex Ohmeda 86 Pilgrim Road Needham, MA 02492

Re: K013246

Trade Name: Datex-Ohmeda S/5 Network and Central '01 Regulation Number: 21 CFR 870.2300 Regulation Name: Network and Communication Physiological System Regulatory Class: Class II (two) Product Code: MSX Dated: September 26, 2001 Received: September 28, 2001

Dear Mr. Kent:

We have reviewed your Section 510(k) premarket notification of intent to market the device we nave to to wowed your becally is the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate 101 use stated in the encreatinent date of the Medical Device Amendments, or to conninered pror to that 2011-17-11, in accordance with the provisions of the Federal Food, Drug, devices that have been recuired in assee approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The I ou may, dicrorolo, mance of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration.

If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it If your device is olassified (600 we controls. Existing major regulations affecting your device can may be subject to sach additions, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.

{6}------------------------------------------------

## Page 2 - Mr. Joel C. Kent

Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must or any I odetar band the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); good manufacturing practice requirements as set Of A rat 0077, accesses (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.

This letter will allow you to begin marketing your device as described in your Section 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally premarket notineated. "The sification for your device and thus, permits your device to proceed to the market.

If you desire specific advice for your device on our labeling regulation (21 CFR Part 801 and 11 Jou desire specific and 10 for in vitro diagnostic devices), please contact the Office of Compliance at [phone]. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at [phone]. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number [phone] or [phone] or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html

Sincerely yours,

Doulla Teth

Bram D. Zuckerman, M.D. Acting Director Division of Cardiovascular and Respiratory Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

{7}------------------------------------------------

510(k) Number (if known): __

Device Name: Datex-Ohmeda S/5 Network and Central '01

K013246

Indications For Use:

The Datex-Ohmeda S/5™ Network and Central transfers information The Datex-Ohmeda 3/5 - Network dha Sossia Costex-Ohmeda monitor
between networked Datex-Ohmeda devices in the Datex-Ohmeda between lietworked Dutox Onation transfer between several Centrals.
It also allows information transfer between severalsed des network. It also anows information namses it allows a networked device Within one DateX-Onmedia monitor news.
to display, store, print and otherwise process information received from other networked devices.

The Datex-Ohmeda S/5™ Central maintains the network connections The Datex-Onmeda S/3 - Gentral manitors and other networked devices
between the Datex-Ohmeda bedside monitors and other networth o between the Datex-Ohmeda society. Furthermore, it coordinates the in Datex-Olimeda monitor noen of ices in the Datex-Olimeda S/5™
transfer of information between devices in the Datex-Olimed Hooped Hoose transfer of Information between the Datex-Ohmeda Network and Hospital Information Systems (HIS).

The Datex-Ohmeda S/5™ Central can be used for remote monitor The Datex-Onlineuu 0/0 - - Ong, viewing or otherwise processing of management, storing, printing, viowing or other networked devices.
information from several bedside monitors or other networked devices.

The Datex-Ohmeda S/5™ ViewStation can be used for remote monitor The Datex-Onlineda 0/3 - - V101 One of otherwise processing of information management, printing, "citions" or other networked devices.

. The Datex-Olimeda S/5™ Network will be used for patients in the hospital and it is meant for continuous use.

The device is for use by qualified personnel only.

# (PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED)

# Concurrence of CDRH, Office of Device Evaluation (ODE)

| Prescription Use | <div> <span style="text-decoration: overline;"></span> <span style="float: right;">X</span> </div> |
|----------------------|----------------------------------------------------------------------------------------------------|
| (Per 21 CFR 801.109) | |

OR

Over-The-Counter Use _

(Optional Format 1-2-96)

**Division of Cardiovascular & Respiratory Devices**
510(k) Number K013246