Clearance Summary
INBODY 770, INBODY 570, INBODY S10, INBODY H20/INBODY H20(B) received FDA 510(k) clearance under submission number K123228, sponsored by Biospace Corporation Limited. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2013-03-08.
- Submission: K123228
- Applicant / Sponsor: Biospace Corporation Limited
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2770
- Decision date: 2013-03-08
Classification & Regulation
This clearance is catalogued under FDA product code MNW and 21 CFR 870.2770, within the Cardiovascular review panel as a Class II device.