Clearance Summary
TRIAGE CARDIO PROFILER/TRIAGE CARDIAC PANEL received FDA 510(k) clearance under submission number K030286, sponsored by Biosite Incorporated. 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 2003-02-21.
- Submission: K030286
- Applicant / Sponsor: Biosite Incorporated
- Clearance pathway: Special
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1117
- Decision date: 2003-02-21
Classification & Regulation
This clearance is catalogued under FDA product code NBC and 21 CFR 862.1117, within the Clinical Chemistry review panel as a Class II device.