Clearance Summary
EPIDURAL CATHETER WITH CONNECTOR (AND ACCESSORY) received FDA 510(k) clearance under submission number K010425, sponsored by Hdc Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2001-03-15.
- Submission: K010425
- Applicant / Sponsor: Hdc Corp.
- Clearance pathway: Special
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.4160
- Decision date: 2001-03-15
Classification & Regulation
This clearance is catalogued under FDA product code KNF and 21 CFR 884.4160, within the Obstetrics/Gynecology review panel as a Class II device.