Clearance Summary
ORAGENE-DX OGD-500; ORAGENE-DX OGD-575; ORAGENE-DX OXD-525; ORAGENE-DX OYD-500 received FDA 510(k) clearance under submission number K110701, sponsored by DNA Genotek, Inc.. 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 2011-12-02.
- Submission: K110701
- Applicant / Sponsor: DNA Genotek, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1675
- Decision date: 2011-12-02
Classification & Regulation
This clearance is catalogued under FDA product code OYJ and 21 CFR 862.1675, within the Clinical Chemistry review panel as a Class II device.