Clearance Summary
BODYMETRIX BX2000 received FDA 510(k) clearance under submission number K082147, sponsored by Intelametrix, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2009-03-20.
- Submission: K082147
- Applicant / Sponsor: Intelametrix, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2770
- Decision date: 2009-03-20
Classification & Regulation
This clearance is catalogued under FDA product code OMV and 21 CFR 870.2770, within the Cardiovascular review panel as a Class II device.