Ultrapro Workstation
by Ramsoft Inc
510(k) K942917
Ultrapro Workstation is a Class I device made by Ramsoft Inc, cleared under FDA 510(k) K942917 on 14 Nov 1994, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK942917 | Date14 Nov 1994 | StatusActive |
Official records
- FDA 510(k) database K942917
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- LMD
- FDA applicant
- Ramsoft, Inc.
- Device class
- Class I
- Regulation
- 21 CFR Part 892.2020
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
Similar devices
Other devices filed under FDA product code LMD (System, Digital Image Communications, Radiological).
- STATVIEW by Image Data Corp.
- AMICAS WEB/INTRANET IMAGE SERVER by Autocyt Group, Inc.
- COURIER PC by Shoreline Business Consulting
- IMPAX 5000 by Heraeus Kulzer, Inc.
- GE ADVANTAGE DIGITIZER WORKSTATION by GE MEDICAL SYSTEMS, INC.
- RADMAN IMAGE MANAGMENT SYSTEM by Infocure Systems, Inc.
- SIENET SPI SPOOLER by SIEMENS MEDICAL SOLUTIONS USA, INC.
- INTERFACE MODULES IM 1000 IMAGE COMMUNI-NETWORK by Impact Systems Corp.
- PACSPRO I by Advanced Video Products, Inc.
- Brainlab Origin OR 1.0 by Brainlab SE