Clearance Summary
DIA SCREEN 10 WAY REAGENT STRIPS received FDA 510(k) clearance under submission number K961375, sponsored by Genesis Labs, 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 1996-06-18.
- Submission: K961375
- Applicant / Sponsor: Genesis Labs, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1340
- Decision date: 1996-06-18
Classification & Regulation
This clearance is catalogued under FDA product code JIL and 21 CFR 862.1340, within the Clinical Chemistry review panel as a Class II device.