Clearance Summary
INVERNESS MEDICAL EARLY PREGNANCY TEST received FDA 510(k) clearance under submission number K013907, sponsored by Cambridge Diagnostics Ireland, Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2001-12-18.
- Submission: K013907
- Applicant / Sponsor: Cambridge Diagnostics Ireland, Ltd.
- Clearance pathway: Special
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1155
- Decision date: 2001-12-18
Classification & Regulation
This clearance is catalogued under FDA product code LCX and 21 CFR 862.1155, within the Clinical Chemistry review panel as a Class II device.