Clearance Summary
ACTH IRMA KIT II MITSUBISHI YUKA received FDA 510(k) clearance under submission number K915727, sponsored by Mitsubishi Yuka America, Inc.. 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 1992-03-02.
- Submission: K915727
- Applicant / Sponsor: Mitsubishi Yuka America, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1025
- Decision date: 1992-03-02
Classification & Regulation
This clearance is catalogued under FDA product code CKG and 21 CFR 862.1025, within the Clinical Chemistry review panel as a Class II device.