Clearance Summary
ORCEPAD received FDA 510(k) clearance under submission number K875123, sponsored by Alton Dean Medical, 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 1988-06-21.
- Submission: K875123
- Applicant / Sponsor: Alton Dean Medical, Inc.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.4900
- Decision date: 1988-06-21
Classification & Regulation
This clearance is catalogued under FDA product code HDD and 21 CFR 884.4900, within the Obstetrics/Gynecology review panel as a Class II device.