Clearance Summary
OLYMPUS PREALBUMIN CALIBRATOR, ODR3029 received FDA 510(k) clearance under submission number K032285, sponsored by Olympus America, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2003-08-21.
- Submission: K032285
- Applicant / Sponsor: Olympus America, Inc.
- Clearance pathway: Abbreviated
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1150
- Decision date: 2003-08-21
Classification & Regulation
This clearance is catalogued under FDA product code JIT and 21 CFR 862.1150, within the Clinical Chemistry review panel as a Class II device.