The following data is part of a premarket notification filed by Siemens Medical Solution Usa, Inc. with the FDA for Artis Zee/zeego & Artis Q/q.zen.
| Device ID | K181407 |
| 510k Number | K181407 |
| Device Name: | Artis Zee/zeego & Artis Q/Q.zen |
| Classification | Interventional Fluoroscopic X-ray System |
| Applicant | Siemens Medical Solution USA, Inc. 40 Liberty Boulevard 65-1A Malvern, PA 19355 |
| Contact | Patricia D. Jones |
| Correspondent | Patricia D. Jones Siemens Medical Solution USA, Inc. 40 Liberty Boulevard 65-1A Malvern, PA 19355 |
| Product Code | OWB |
| Subsequent Product Code | IZI |
| Subsequent Product Code | JAA |
| Subsequent Product Code | JAK |
| CFR Regulation Number | 892.1650 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-05-30 |
| Decision Date | 2018-08-15 |
| Summary: | summary |