Clearance Summary
FIBERLASE 100 MEDICAL LASER SYS/ND:YAG MENORRHAGIA received FDA 510(k) clearance under submission number K862444, sponsored by Laser Media. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 1986-09-25.
- Submission: K862444
- Applicant / Sponsor: Laser Media
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.4550
- Decision date: 1986-09-25
Classification & Regulation
This clearance is catalogued under FDA product code HHR and 21 CFR 884.4550, within the Obstetrics/Gynecology review panel as a Class II device.