The following data is part of a premarket notification filed by Sony Electronics, Inc. with the FDA for Sony Digital Printer Up-d898md/sony Hybrid Printer Up-x898md.
| Device ID | K141454 |
| 510k Number | K141454 |
| Device Name: | SONY DIGITAL PRINTER UP-D898MD/SONY HYBRID PRINTER UP-X898MD |
| Classification | Camera, Multi Format, Radiological |
| Applicant | SONY ELECTRONICS, INC. 62 FOREST ST. STE 300 Marlborough, MA 01752 |
| Contact | Joanne Bronikowski |
| Correspondent | Joanne Bronikowski SONY ELECTRONICS, INC. 62 FOREST ST. STE 300 Marlborough, MA 01752 |
| Product Code | LMC |
| CFR Regulation Number | 892.2040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-06-02 |
| Decision Date | 2014-06-26 |
| Summary: | summary |