Clearance Summary
DSL ACTIVE T4 EIA received FDA 510(k) clearance under submission number K971269, sponsored by Diagnostic Systems Laboratories, 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 1997-05-22.
- Submission: K971269
- Applicant / Sponsor: Diagnostic Systems Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1700
- Decision date: 1997-05-22
Classification & Regulation
This clearance is catalogued under FDA product code KLI and 21 CFR 862.1700, within the Clinical Chemistry review panel as a Class II device.