Clearance Summary
OCTAX LASER SHOT SYSTEM received FDA 510(k) clearance under submission number K062524, sponsored by Minitube of America, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2006-12-15.
- Submission: K062524
- Applicant / Sponsor: Minitube of America, Inc.
- Clearance pathway: Abbreviated
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.6200
- Decision date: 2006-12-15
Classification & Regulation
This clearance is catalogued under FDA product code MRX and 21 CFR 884.6200, within the Obstetrics/Gynecology review panel as a Class II device.