Clearance Summary
NOVA 16 ANALYZER (MODIFICATION POINT OF CARE USAGE) received FDA 510(k) clearance under submission number K963005, sponsored by Nova Biomedical 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 1996-08-23.
- Submission: K963005
- Applicant / Sponsor: Nova Biomedical Corp.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1160
- Decision date: 1996-08-23
Classification & Regulation
This clearance is catalogued under FDA product code JFL and 21 CFR 862.1160, within the Clinical Chemistry review panel as a Class II device.