The following data is part of a premarket notification filed by Medical Diagnostic Technologies, Inc. with the FDA for Ctc Workstation, Model 2200.
Device ID | K062229 |
510k Number | K062229 |
Device Name: | CTC WORKSTATION, MODEL 2200 |
Classification | System, Image Processing, Radiological |
Applicant | MEDICAL DIAGNOSTIC TECHNOLOGIES, INC. 8960 W TROPICANA AVE SUITE 700 Las Vegas, NV 89147 |
Contact | James M Benson |
Correspondent | James M Benson MEDICAL DIAGNOSTIC TECHNOLOGIES, INC. 8960 W TROPICANA AVE SUITE 700 Las Vegas, NV 89147 |
Product Code | LLZ |
CFR Regulation Number | 892.2050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-08-02 |
Decision Date | 2006-09-11 |
Summary: | summary |