510(k) K141454
K141454 is an FDA 510(k) premarket notification submitted by Sony Electronics, Inc. for the device "SONY DIGITAL PRINTER UP-D898MD/SONY HYBRID PRINTER UP-X898MD". The FDA issued a decision of Substantially Equivalent on June 26, 2014. The device falls under product code LMC (Camera, Multi Format, Radiological), a Class II device regulated under 21 CFR 892.2040. Sony Electronics, Inc. has at least 7 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 26, 2014
- Date Received
- June 2, 2014
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Camera, Multi Format, Radiological
- Device Class
- Class II
- Regulation Number
- 892.2040
- Review Panel
- RA
- Submission Type