Clearance Summary
Z-NET received FDA 510(k) clearance under submission number K001003, sponsored by Demite Limited. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2001-12-10.
- Submission: K001003
- Applicant / Sponsor: Demite Limited
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6190
- Decision date: 2001-12-10
Classification & Regulation
This clearance is catalogued under FDA product code FMW and 21 CFR 880.6190, within the General Hospital review panel as a Class I device.