Clearance Summary
ACA CREATINE KINASE ISOENZYMES received FDA 510(k) clearance under submission number K790088, sponsored by E.I. Dupont DE Nemours & Co., 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 1979-03-12.
- Submission: K790088
- Applicant / Sponsor: E.I. Dupont DE Nemours & Co., Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1215
- Decision date: 1979-03-12
Classification & Regulation
This clearance is catalogued under FDA product code JHS and 21 CFR 862.1215, within the Clinical Chemistry review panel as a Class II device.