Clearance Summary
ARTIS 3200 DIAGNOSTIC ULTRASOUND DEVICE received FDA 510(k) clearance under submission number K875251, sponsored by Philips Medical Systems (Cleveland), Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1988-05-11.
- Submission: K875251
- Applicant / Sponsor: Philips Medical Systems (Cleveland), Inc.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1560
- Decision date: 1988-05-11
Classification & Regulation
This clearance is catalogued under FDA product code IYO and 21 CFR 892.1560, within the Radiology review panel as a Class II device.