Clearance Summary
NEWTOM QR-DVT 9000 received FDA 510(k) clearance under submission number K003787, sponsored by Aperio Services, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2001-03-08.
- Submission: K003787
- Applicant / Sponsor: Aperio Services, LLC
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1750
- Decision date: 2001-03-08
Classification & Regulation
This clearance is catalogued under FDA product code OAS and 21 CFR 892.1750, within the Radiology review panel as a Class II device.