The following data is part of a premarket notification filed by Siemens Medical Solutions Usa, Inc. with the FDA for Multix Top/pro Radiographic X-ray Table.
| Device ID | K971452 |
| 510k Number | K971452 |
| Device Name: | MULTIX TOP/PRO RADIOGRAPHIC X-RAY TABLE |
| Classification | Table, Radiographic, Non-tilting, Powered |
| Applicant | SIEMENS MEDICAL SOLUTIONS USA, INC. 186 WOOD AVE. SOUTH Iselin, NJ 08830 |
| Contact | Jeffrey W Koontz |
| Correspondent | Jeffrey W Koontz SIEMENS MEDICAL SOLUTIONS USA, INC. 186 WOOD AVE. SOUTH Iselin, NJ 08830 |
| Product Code | IZZ |
| CFR Regulation Number | 892.1980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-04-21 |
| Decision Date | 1997-05-14 |
| Summary: | summary |