Clearance Summary
KODAK EKTACHEM DTII SYSTEM received FDA 510(k) clearance under submission number K912844, sponsored by Eastman Kodak Company. 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 1991-09-04.
- Submission: K912844
- Applicant / Sponsor: Eastman Kodak Company
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.2160
- Decision date: 1991-09-04
Classification & Regulation
This clearance is catalogued under FDA product code JJE and 21 CFR 862.2160, within the Clinical Chemistry review panel as a Class I device.