Clearance Summary
TROCAR AND CANNULA ACCESSORY received FDA 510(k) clearance under submission number K945741, sponsored by Applied Medical Resources. 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 1995-02-28.
- Submission: K945741
- Applicant / Sponsor: Applied Medical Resources
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.1720
- Decision date: 1995-02-28
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.