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 |