Clearance Summary
SCANDIA-45 GAMMA CAMERA SYSTEM received FDA 510(k) clearance under submission number K101391, sponsored by Scandia Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2010-08-04.
- Submission: K101391
- Applicant / Sponsor: Scandia Corporation
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class I
- Regulation citation: 21 CFR 892.1100
- Decision date: 2010-08-04
Classification & Regulation
This clearance is catalogued under FDA product code IYX and 21 CFR 892.1100, within the Radiology review panel as a Class I device.