Clearance Summary
VITROS IMMUNODIAGNOSTIC PRODUCTS HBSAG CONTROLS received FDA 510(k) clearance under submission number K030067, sponsored by Ortho-Clinical Diagnostics. 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 2003-01-17.
- Submission: K030067
- Applicant / Sponsor: Ortho-Clinical Diagnostics
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1660
- Decision date: 2003-01-17
Classification & Regulation
This clearance is catalogued under FDA product code MJX and 21 CFR 862.1660, within the Clinical Chemistry review panel as a Class I device.