Clearance Summary
HDL-EX SEIKEN ASSAY KIT received FDA 510(k) clearance under submission number K041090, 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 2004-10-29.
- Submission: K041090
- Applicant / Sponsor: Denka Seiken Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1475
- Decision date: 2004-10-29
Classification & Regulation
This clearance is catalogued under FDA product code LBS and 21 CFR 862.1475, within the Clinical Chemistry review panel as a Class I device.