Clearance Summary
DPD-12PCC received FDA 510(k) clearance under submission number K990734, sponsored by Scanditronix Medical AB. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1999-05-28.
- Submission: K990734
- Applicant / Sponsor: Scanditronix Medical AB
- Clearance pathway: Special
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.5050
- Decision date: 1999-05-28
Classification & Regulation
This clearance is catalogued under FDA product code IYE and 21 CFR 892.5050, within the Radiology review panel as a Class II device.