Clearance Summary
CRP (II) CALIBRATORS received FDA 510(k) clearance under submission number K030546, sponsored by Denka Seiken Co., Ltd.. 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 2003-06-02.
- Submission: K030546
- Applicant / Sponsor: Denka Seiken Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1150
- Decision date: 2003-06-02
Classification & Regulation
This clearance is catalogued under FDA product code JIS and 21 CFR 862.1150, within the Clinical Chemistry review panel as a Class II device.