510(k) K083522
K083522 is an FDA 510(k) premarket notification submitted by Sony Electronics, Inc. for the device "SONY UP-DF750 DIGITAL FILM IMAGER". The FDA issued a decision of Substantially Equivalent on January 9, 2009. 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
- January 9, 2009
- Date Received
- November 26, 2008
- 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