Clearance Summary
VMA EIA KIT YAMASA received FDA 510(k) clearance under submission number K895287, sponsored by Yamasa Shoy 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 1989-10-30.
- Submission: K895287
- Applicant / Sponsor: Yamasa Shoy Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1795
- Decision date: 1989-10-30
Classification & Regulation
This clearance is catalogued under FDA product code CDF and 21 CFR 862.1795, within the Clinical Chemistry review panel as a Class I device.