Clearance Summary
FIBERLASE II ND:YAG LASER FOR TREAT OF MENORRHAGIA received FDA 510(k) clearance under submission number K872352, 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 1987-12-30.
- Submission: K872352
- Applicant / Sponsor: Laser Media
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.4550
- Decision date: 1987-12-30
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.