Clearance Summary
HUMAN LYME EIA FOR THE DETECT OF ANTIBODIES received FDA 510(k) clearance under submission number K890281, sponsored by Cambridge Bioscience Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 1989-03-15.
- Submission: K890281
- Applicant / Sponsor: Cambridge Bioscience Corp.
- Clearance pathway: Traditional
- Review panel: Microbiology
- Device class: Class II
- Regulation citation: 21 CFR 866.3830
- Decision date: 1989-03-15
Classification & Regulation
This clearance is catalogued under FDA product code LSR and 21 CFR 866.3830, within the Microbiology review panel as a Class II device.