Clearance Summary
RAPID AUTOMATIC PNEUMOPERITONEUM-I received FDA 510(k) clearance under submission number K900808, sponsored by Trek Medical Products, 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 1990-09-19.
- Submission: K900808
- Applicant / Sponsor: Trek Medical Products, Inc.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.1730
- Decision date: 1990-09-19
Classification & Regulation
This clearance is catalogued under FDA product code HIF and 21 CFR 884.1730, within the Obstetrics/Gynecology review panel as a Class II device.