Clearance Summary
PANBUS DIGITAL EEG & SLEEP ACQUISITION DEVICES received FDA 510(k) clearance under submission number K042364, sponsored by Lamont Medical, 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 2004-09-30.
- Submission: K042364
- Applicant / Sponsor: Lamont Medical, Inc.
- Clearance pathway: Special
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.1400
- Decision date: 2004-09-30
Classification & Regulation
This clearance is catalogued under FDA product code OLV and 21 CFR 882.1400, within the Neurology review panel as a Class II device.