DICOM THEATER
System, Image Processing, Radiological
FERGUSON MEDICAL
The following data is part of a premarket notification filed by Ferguson Medical with the FDA for Dicom Theater.
Pre-market Notification Details
| Device ID | K033153 |
| 510k Number | K033153 |
| Device Name: | DICOM THEATER |
| Classification | System, Image Processing, Radiological |
| Applicant | FERGUSON MEDICAL 12200 ACADEMY ROAD NE #931 Albuquerque, NM 87111 |
| Contact | Frank Ferguson |
| Correspondent | Frank Ferguson FERGUSON MEDICAL 12200 ACADEMY ROAD NE #931 Albuquerque, NM 87111 |
| Product Code | LLZ |
| CFR Regulation Number | 892.2050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-09-30 |
| Decision Date | 2004-04-23 |
| Summary: | summary |
Trademark Results [DICOM THEATER]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 DICOM THEATER 79001998 not registered Dead/Abandoned |
BARCO N.V. 2004-02-27 |
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