Clearance Summary
NOVA MAX MINI BLOOD GLUCOSE AND B-KETONE MONITOR received FDA 510(k) clearance under submission number K122688, sponsored by Nova Biomedical Corporation. 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 2013-04-04.
- Submission: K122688
- Applicant / Sponsor: Nova Biomedical Corporation
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1345
- Decision date: 2013-04-04
Classification & Regulation
This clearance is catalogued under FDA product code LFR and 21 CFR 862.1345, within the Clinical Chemistry review panel as a Class II device.