Clearance Summary
300LC ULTRASOUND IMAGING SYSTEMS, MODEL 300LC received FDA 510(k) clearance under submission number K002880, sponsored by Pie Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2000-10-26.
- Submission: K002880
- Applicant / Sponsor: Pie Medical
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1550
- Decision date: 2000-10-26
Classification & Regulation
This clearance is catalogued under FDA product code IYN and 21 CFR 892.1550, within the Radiology review panel as a Class II device.