Sony Digital Printer UP-D898MD/SONY Hybrid Printer UP-X898MD
FDA 510(k) K141454 · Sony Electronics, Inc.
510(k) numberK141454
Submission
- Device name
- Sony Digital Printer UP-D898MD/SONY Hybrid Printer UP-X898MD
- Applicant
- Sony Electronics, Inc.
Marlborough, MA, US - Received
- June 2, 2014
- Decision date
- June 26, 2014
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
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| K141346 | Sony Hybird Graphic UP-971AD, Sony Hybird Graphic Printer UP-991ADLMC · Traditional | 06/26/2014SE |
| K120611 | Sony PVM-2551MD Oled MonitorGCJ · Traditional | 06/28/2012SE |
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Questions and answers
When was Sony Digital Printer UP-D898MD/SONY Hybrid Printer UP-X898MD cleared by the FDA?
Sony Digital Printer UP-D898MD/SONY Hybrid Printer UP-X898MD (K141454) received a 510(k) decision of Substantially Equivalent on June 26, 2014, 24 days after the submission was received.
What is the product code of K141454?
The FDA product code is LMC – Camera, Multi Format, Radiological, a Class II (moderate risk) device regulated under 21 CFR 892.2040.