The following data is part of a premarket notification filed by Pyramid Medical, Inc. with the FDA for Digital Imager.
| Device ID | K032022 | 
| 510k Number | K032022 | 
| Device Name: | DIGITAL IMAGER | 
| Classification | Digitizer, Image, Radiological | 
| Applicant | PYRAMID MEDICAL, INC. 10940 PORTAL MEDICAL DR. Los Alamitos, CA 90720 | 
| Contact | Claude Bennett | 
| Correspondent | Claude Bennett PYRAMID MEDICAL, INC. 10940 PORTAL MEDICAL DR. Los Alamitos, CA 90720 | 
| Product Code | LMA | 
| CFR Regulation Number | 892.2030 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2003-06-30 | 
| Decision Date | 2003-09-02 | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  DIGITAL IMAGER  78790246  3246676 Dead/Cancelled | Sharp Kabushiki Kaisha 2006-01-12 | 
|  DIGITAL IMAGER  78790232  not registered Dead/Abandoned | Sharp Kabushiki Kaisha a/t/a Sharp Corporation 2006-01-12 | 
|  DIGITAL IMAGER  76571990  not registered Dead/Abandoned | SHARP KABUSHIKI KAISHA 2004-01-27 | 
|  DIGITAL IMAGER  76571989  not registered Dead/Abandoned | SHARP KABUSHIKI KAISHA 2004-01-27 |