Clearance Summary
GALILEO ARTHROSCOPES received FDA 510(k) clearance under submission number K934707, sponsored by Galileo Electro-Optics Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1994-10-07.
- Submission: K934707
- Applicant / Sponsor: Galileo Electro-Optics Corp.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.1100
- Decision date: 1994-10-07
Classification & Regulation
This clearance is catalogued under FDA product code HRX and 21 CFR 888.1100, within the Orthopedic review panel as a Class II device.