Clearance Summary
CREATINE KINASE LIQUID REAGENT, MODEL C519-440 received FDA 510(k) clearance under submission number K072548, sponsored by Teco 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 2008-04-18.
- Submission: K072548
- Applicant / Sponsor: Teco Diagnostics
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1215
- Decision date: 2008-04-18
Classification & Regulation
This clearance is catalogued under FDA product code CGS and 21 CFR 862.1215, within the Clinical Chemistry review panel as a Class II device.