Clearance Summary
CO2 RIGID LASER ENDOSCOPE PROBE SERIES 792/LAPARO received FDA 510(k) clearance under submission number K881010, sponsored by Sharplan Lasers, Inc.. 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 1988-04-21.
- Submission: K881010
- Applicant / Sponsor: Sharplan Lasers, Inc.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.1720
- Decision date: 1988-04-21
Classification & Regulation
This clearance is catalogued under FDA product code HET and 21 CFR 884.1720, within the Obstetrics/Gynecology review panel as a Class II device.