Clearance Summary
OLYMPUS LYOPHILIZED CALIBRATOR, MODELS DR0070 AND DR0071 received FDA 510(k) clearance under submission number K032665, 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 2003-11-21.
- Submission: K032665
- Applicant / Sponsor: Olympus America, Inc.
- Clearance pathway: Abbreviated
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1150
- Decision date: 2003-11-21
Classification & Regulation
This clearance is catalogued under FDA product code JIX and 21 CFR 862.1150, within the Clinical Chemistry review panel as a Class II device.