OLYMPUS COMM. NTWK., SC 3000 WKST. & REMOTE DISPLAY, R 100 RECORDER
Device Facts
| Record ID | K955059 |
|---|---|
| Device Name | OLYMPUS COMM. NTWK., SC 3000 WKST. & REMOTE DISPLAY, R 100 RECORDER |
| Applicant | Siemens Medical Solutions USA, Inc. |
| Product Code | DSI · Cardiovascular |
| Decision Date | Jun 7, 1996 |
| Decision | SESE |
| Submission Type | Traditional |
| Regulation | 21 CFR 870.1025 |
| Device Class | Class 2 |
Intended Use
Olympus Communications Network: To act as a communications network for the SC 9000/9015 (K946306) and SC 6000/6000P (K944350) Patient Monitoring Systems, the SC 3000 Workstation, R 50 (K944350) and R 100 Recorders, and laser printers. SC 3000 Workstation: To act as a central monitoring device for the SC 9000/9015 (K946306) and SC 6000/6000P (K944350) Patient Monitoring Systems through its connection to the Siemens Olympus Communications Network. SC 3000 Remote Display: To act as a Slave Display for the SC 3000 Workstation.
Device Story
System comprises Olympus Communications Network, SC 3000 Workstation, and SC 3000 Remote Display. Network facilitates data communication between patient monitors (SC 9000/9015, SC 6000/6000P), recorders, and printers. SC 3000 Workstation functions as central monitoring hub, aggregating patient data from connected monitors for clinician review. SC 3000 Remote Display acts as slave unit for workstation. Used in clinical settings by healthcare professionals to monitor patient physiological data. System enables centralized oversight of patient status, supporting clinical decision-making through real-time data display and alarm management.
Clinical Evidence
Bench testing only. No clinical data provided. Safety and effectiveness demonstrated through compliance with electrical safety standards (IEC 601-1, UL 544, UL 433, UL 1950, EN 60950, CSA 22.2 No. 950) and internal qualification testing against product specifications.
Technological Characteristics
Networked patient monitoring system. Components include communications network, central workstation, and remote display. Electrical safety compliance: IEC 601-1, UL 544, UL 433, UL 1950, EN 60950, CSA 22.2 No. 950. Connectivity: Networked system for data transmission between monitors, recorders, and printers. CE marked.
Indications for Use
Indicated for use as a communications network, central monitoring station, and remote display for patient monitoring systems (SC 9000/9015 and SC 6000/6000P) in clinical environments.
Regulatory Classification
Identification
The arrhythmia detector and alarm device monitors an electrocardiogram and is designed to produce a visible or audible signal or alarm when atrial or ventricular arrhythmia, such as premature contraction or ventricular fibrillation, occurs.
Special Controls
*Classification.* Class II (special controls). The guidance document entitled “Class II Special Controls Guidance Document: Arrhythmia Detector and Alarm” will serve as the special control. See § 870.1 for the availability of this guidance document.
Predicate Devices
- SIRENET Communications Network (K920445)
- Unity Network (K900598, K901072, K912799)
- SIRECUST 120/121C Central Station (K920445)
- SIRECUST 120/121S Slave Display (K920445)
- CentralScope 12 Central Station (K901072)
- Remote Color Display (K901884)
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