Clearance Summary
BOD POD received FDA 510(k) clearance under submission number K060848, sponsored by Life Measurement, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2006-06-27.
- Submission: K060848
- Applicant / Sponsor: Life Measurement, Inc.
- Clearance pathway: Abbreviated
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2770
- Decision date: 2006-06-27
Classification & Regulation
This clearance is catalogued under FDA product code OAC and 21 CFR 870.2770, within the Cardiovascular review panel as a Class II device.