Clearance Summary
BUEHLMANN LAB AS, ACE ANGIO CONV ENZYME KIN ASSAY received FDA 510(k) clearance under submission number K913091, sponsored by American Laboratory Products 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 1991-08-26.
- Submission: K913091
- Applicant / Sponsor: American Laboratory Products Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1090
- Decision date: 1991-08-26
Classification & Regulation
This clearance is catalogued under FDA product code KQN and 21 CFR 862.1090, within the Clinical Chemistry review panel as a Class II device.