Clearance Summary
SAMPLOK received FDA 510(k) clearance under submission number K000777, sponsored by Itl Corporation Pty, 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 2000-04-11.
- Submission: K000777
- Applicant / Sponsor: Itl Corporation Pty, Ltd.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1675
- Decision date: 2000-04-11
Classification & Regulation
This clearance is catalogued under FDA product code JKA and 21 CFR 862.1675, within the Clinical Chemistry review panel as a Class II device.