Clearance Summary
QSI 9000 received FDA 510(k) clearance under submission number K894560, sponsored by Quantified Signal Imaging, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1990-08-08.
- Submission: K894560
- Applicant / Sponsor: Quantified Signal Imaging, Inc.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.1870
- Decision date: 1990-08-08
Classification & Regulation
This clearance is catalogued under FDA product code GWF and 21 CFR 882.1870, within the Neurology review panel as a Class II device.