Clearance Summary
BODY COMPOSITION ANALYZER, MODEL: IOI 353 received FDA 510(k) clearance under submission number K092431, sponsored by Jawon Medical Co., Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2009-10-08.
- Submission: K092431
- Applicant / Sponsor: Jawon Medical Co., Ltd.
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2770
- Decision date: 2009-10-08
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.