Data / Medical devices / United States / CNMC Co., Inc.
CNMC Co., Inc.: FDA-registered device maker in Nashville, TN, United States, 3 510(k) clearances
CNMC Co., Inc. is registered with the FDA (registration 3006073271) in Nashville, TN, United States. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated August 7, 2018. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3006073271
- Address
- 865 Easthagen Dr, Nashville, TN, United States, 37217
- Owner or operator
- CNMC Co., Inc. (10038474)
- Roles
- Manufacturer, Repackager or relabeler
- First device listed
- September 3, 2015
- Registered through
- 2026
- Brand names listed
- Equidose II, Model 206 Electrometer/Dosimeter, WP-3040 1D Water Phantom, WP-3840 1D Water Phantom
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accelerator, Linear, Medical | IYE | 2 | Manufacturer | accessdata.fda.gov |
| System, Nuclear Magnetic Resonance Imaging | LNH | 2 | Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| August 7, 2018 | K173848 | Model WP-3840 and WP-3040 | IYE | Substantially Equivalent | Cnmc Co., Inc. | accessdata.fda.gov |
| September 3, 2015 | K150265 | Model 206 Electrometer/Dosimeter | IYE | Substantially Equivalent | Cnmc Company Incorporated | accessdata.fda.gov |
| June 6, 2001 | K011466 | QED DIODE DETECTORS, MODELS 1112-1116 | LNH | Substantially Equivalent | Sun Nuclear Corp. | accessdata.fda.gov |
Compare with other makers
Updated August 7, 2018. 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.