Clearance Summary
NAVIGATOR APPLICATIONS SUITE received FDA 510(k) clearance under submission number K102389, sponsored by GE Healthcare Finland Oy. The device was reviewed via the Special premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2011-06-10.
- Submission: K102389
- Applicant / Sponsor: GE Healthcare Finland Oy
- Clearance pathway: Special
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.5160
- Decision date: 2011-06-10
Classification & Regulation
This clearance is catalogued under FDA product code BSZ and 21 CFR 868.5160, within the Anesthesiology review panel as a Class II device.