Data / Medical devices / Mexico / Compania Mexicana De Radiologia CGR, S.A. De C.V.
Compania Mexicana De Radiologia CGR, S.A. De C.V.: FDA-registered device maker in Queretaro, Mexico, 4 510(k) clearances
Compania Mexicana De Radiologia CGR, S.A. De C.V. is registered with the FDA (registration 3004756607) in Queretaro, Mexico. It lists 6 device types. The FDA files 4 510(k) clearances under its listings, the newest dated January 28, 2020. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3004756607
- Address
- Municlpio El Marques, Queretaro, Mexico, 76240
- Owner or operator
- CMR X-Ray, LLC (9053481)
- Roles
- Manufacturer
- First device listed
- May 10, 2005
- Registered through
- 2026
- Brand names listed
- ARiX RAD Acquisition Console, ARiX RAD System, CP IV, CP V, GMX AF II, MRH ALPHA, MRH II & MRH IIE RADIOGRAPHIC SYSTEMS, MRH E IV, MRH III E and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Generator, High-Voltage, X-Ray, Diagnostic | IZO | 1 | Manufacturer | accessdata.fda.gov |
| Holder, Radiographic Cassette, Wall-Mounted | IXY | 1 | Manufacturer | accessdata.fda.gov |
| System, Image Processing, Radiological | LLZ | 2 | Manufacturer | accessdata.fda.gov |
| System, X-Ray, Stationary | KPR | 2 | Manufacturer | accessdata.fda.gov |
| Table, Radiologic | KXJ | 2 | Manufacturer | accessdata.fda.gov |
| Tube Mount, X-Ray, Diagnostic | IYB | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| January 28, 2020 | K193637 | MRH ALFA Radiographic System, MRH II Radiographic System, MRH IIE Radiographic System | KPR | Substantially Equivalent | Compania Mexicana DE Radiologia Cgr, S.A. DE C.V. | accessdata.fda.gov |
| November 26, 2018 | K182134 | ARiX RAD Radiographic System | KPR | Substantially Equivalent | Compania Mexicana DE Radiologia Cgr, S.A. DE C.V. | accessdata.fda.gov |
| August 17, 2016 | K161518 | PACS CORE/ENCORE | LLZ | Substantially Equivalent | Compania Mexicana DE Radiologia Cgr, S.A. DE C.V. | accessdata.fda.gov |
| February 20, 2013 | K123650 | ARIX RAD ACQUISITION CONSOLE | LLZ | Substantially Equivalent | Compania Mexicana DE Radiologia Cgr, S.A. DE C.V. | accessdata.fda.gov |
Compare with other makers
- All makers of Holder, Radiographic Cassette, Wall-Mounted
- All makers of Generator, High-Voltage, X-Ray, Diagnostic
- All makers of System, X-Ray, Stationary
- All makers of System, Image Processing, Radiological
- All makers of Tube Mount, X-Ray, Diagnostic
- All makers of Table, Radiologic
Updated January 28, 2020. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.