Clearance Summary
ProxiDiagnost N90 / Precision CRF (706110, 706400) received FDA 510(k) clearance under submission number K233945, sponsored by Philips Medical Systems Dmc GmbH. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2024-01-11.
- Submission: K233945
- Applicant / Sponsor: Philips Medical Systems Dmc GmbH
- Clearance pathway: Special
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1650
- Decision date: 2024-01-11
Classification & Regulation
This clearance is catalogued under FDA product code JAA and 21 CFR 892.1650, within the Radiology review panel as a Class II device.