Seemor - Display & Processing Program Executing on Personal Computer System
510(k) K973653
Active
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK973653 | Date12 Dec 1997 | StatusActive |
Recalls
No FDA recalls found in the data synced 22 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA Product Code
- LLZ
- Device Class
- Class II
- Regulation
- 21 CFR Part 892.2050
- Advisory Committee
- Radiology
- FDA Decision
- SESE Substantially Equivalent
Overview
AI-generated summary, 6 Oct 2026
Seemor is a software program designed for personal computers to view and manipulate diagnostic medical images. It accepts medical image data as input and provides various tools for image processing, including clipping, window/level adjustment, magnification, pan, cine, and image orientation controls.
This software is intended for use on IBM PC or Macintosh systems. It has received FDA 510(k) clearance under the product code LLZ and is classified as a system for radiological image processing.
Other devices from Areeda Assoc., Ltd.
Questions
AI-generated answers, 6 Oct 2026
What is the intended use of the Seemor software?
Seemor is a software program designed to run on personal computers, specifically IBM PC or Macintosh systems, to view and manipulate diagnostic medical images.
What image processing tools are included in the Seemor program?
The software provides a suite of image processing tools including magnification, pan, cine, image orientation controls, and clipping, as well as window and level adjustments for diagnostic viewing.
What is the regulatory status of the Seemor software?
Seemor has received FDA 510(k) clearance under product code LLZ and is classified as a system for radiological image processing.