Clearance Summary
MODIFICATION TO INTEL HEALTH GUIDE PHS6000 received FDA 510(k) clearance under submission number K101178, sponsored by Intel Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2010-06-29.
- Submission: K101178
- Applicant / Sponsor: Intel Corp.
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2910
- Decision date: 2010-06-29
Classification & Regulation
This clearance is catalogued under FDA product code DRG and 21 CFR 870.2910, within the Cardiovascular review panel as a Class II device.