DOCTORS REVIEW SYSTEM
Device Facts
| Record ID | K970402 |
|---|---|
| Device Name | DOCTORS REVIEW SYSTEM |
| Applicant | Digisonics, Inc. |
| Product Code | LLZ · Radiology |
| Decision Date | Mar 26, 1997 |
| Decision | SESE |
| Submission Type | Traditional |
| Regulation | 21 CFR 892.2050 |
| Device Class | Class 2 |
| Attributes | Software as a Medical Device |
Intended Use
The Doctors Review System (DRS) is general purpose, standalone software for creating patient reports. It consists of Digisonics word processing software together with off-the-shelf computer equipment (PC, VCR, printer, etc.). Using the system, the physician reviews data (from other sources), notes clinical observations from sets of menus, and creates patient reports. Optional analysis programs are provided for quantitation of echo and cath lab data. No diagnoses are made by the software. It is not used for therapy or patient monitoring.
Device Story
Standalone software system for clinical report generation; inputs include data from external sources (echo/cath lab) and manual clinical observations via menu selection; optional modules for echo/cath lab data quantitation and digital image management; operates on PC-based hardware; used by physicians (radiologists, cardiologists, OB/GYN) in hospitals/clinics; facilitates efficient review and reporting; does not provide automated diagnosis, therapy, or patient monitoring; includes database search functionality for stored reports.
Clinical Evidence
Bench testing only. Software verification and validation performed at module, integration, and system levels per internal protocols. Results confirmed software performance satisfies functional and system specifications.
Technological Characteristics
Standalone software; PC-based hardware; optional digital image management and database search modules; connectivity via links to ultrasound systems; menu-driven reporting interface; quantitation algorithms for echo/cath lab data.
Indications for Use
Indicated for use by radiologists, cardiologists, obstetricians, and gynecologists in hospitals, outpatient clinics, and clinical environments for patient report creation and data review.
Regulatory Classification
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).
Reference Devices
- ATL Nova Microsonics - Image Vue DCR System
- TomTec - TomTec 90 with Echocardiography Offline Review
- General Electric - RT 4000 Data Management Center
- On-Time Medical - Click*View
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