Clearance Summary
PATHFAST CK-MB-II CALIBRATORS received FDA 510(k) clearance under submission number K130628, sponsored by Mitsubishi Chemical Medience Corporation. 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 2013-10-04.
- Submission: K130628
- Applicant / Sponsor: Mitsubishi Chemical Medience Corporation
- Clearance pathway: Special
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1150
- Decision date: 2013-10-04
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.