Clearance Summary
SCINTILLATION GAMMA CAMERA received FDA 510(k) clearance under submission number K140206, sponsored by Ddd-Diagnostic A/S. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2014-05-08.
- Submission: K140206
- Applicant / Sponsor: Ddd-Diagnostic A/S
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1200
- Decision date: 2014-05-08
Classification & Regulation
This clearance is catalogued under FDA product code KPS and 21 CFR 892.1200, within the Radiology review panel as a Class II device.