Clearance Summary
5.0 MHZ INTRACAVITARY SECTOR PROBE received FDA 510(k) clearance under submission number K853711, sponsored by General Electric Co.. 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 1985-12-18.
- Submission: K853711
- Applicant / Sponsor: General Electric Co.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.2225
- Decision date: 1985-12-18
Classification & Regulation
This clearance is catalogued under FDA product code HEM and 21 CFR 884.2225, within the Obstetrics/Gynecology review panel as a Class II device.