Clearance Summary
Z-BOX received FDA 510(k) clearance under submission number K030764, sponsored by Z-Kat, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2003-04-24.
- Submission: K030764
- Applicant / Sponsor: Z-Kat, Inc.
- Clearance pathway: Special
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.4560
- Decision date: 2003-04-24
Classification & Regulation
This clearance is catalogued under FDA product code HAW and 21 CFR 882.4560, within the Neurology review panel as a Class II device.