The following data is part of a premarket notification filed by Planmed Oy with the FDA for Mobile Sophie Modification.
| Device ID | K934373 |
| 510k Number | K934373 |
| Device Name: | MOBILE SOPHIE MODIFICATION |
| Classification | System, X-ray, Mammographic |
| Applicant | PLANMED OY ASENTAJANKATU 6 Helsinki, FI 00880 |
| Contact | Sari Myllyrinne |
| Correspondent | Sari Myllyrinne PLANMED OY ASENTAJANKATU 6 Helsinki, FI 00880 |
| Product Code | IZH |
| CFR Regulation Number | 892.1710 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-09-08 |
| Decision Date | 1994-04-07 |