Clearance Summary
KET-1 Blood Ketone Monitoring System received FDA 510(k) clearance under submission number K182593, sponsored by Apex BioTechnology Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2018-12-18.
- Submission: K182593
- Applicant / Sponsor: Apex BioTechnology Corp.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1435
- Decision date: 2018-12-18
Classification & Regulation
This clearance is catalogued under FDA product code JIN and 21 CFR 862.1435, within the Clinical Chemistry review panel as a Class I device.