Clearance Summary
CENTURION PRESSURE INJECTABLE EXTENSION SET received FDA 510(k) clearance under submission number K103562, sponsored by Centurion Medical Products Corporation. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2011-06-23.
- Submission: K103562
- Applicant / Sponsor: Centurion Medical Products Corporation
- Clearance pathway: Abbreviated
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5440
- Decision date: 2011-06-23
Classification & Regulation
This clearance is catalogued under FDA product code FPA and 21 CFR 880.5440, within the General Hospital review panel as a Class II device.