The following data is part of a premarket notification filed by Cnmc Co., Inc. with the FDA for Model Wp-3840 And Wp-3040.
| Device ID | K173848 |
| 510k Number | K173848 |
| Device Name: | Model WP-3840 And WP-3040 |
| Classification | Accelerator, Linear, Medical |
| Applicant | CNMC Co., Inc. 865 Easthagen Drive Nashville, TN 37217 |
| Contact | Thomas Kraus |
| Correspondent | Thomas Kraus CNMC Co., Inc. 865 Easthagen Drive Nashville, TN 37217 |
| Product Code | IYE |
| CFR Regulation Number | 892.5050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-12-19 |
| Decision Date | 2018-08-07 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00860321001410 | K173848 | 000 |
| 00860321001403 | K173848 | 000 |