Clearance Summary
SMARTSITE VENTED VIAL ACCESS DEVICE, MODEL TBD received FDA 510(k) clearance under submission number K052790, sponsored by Cardinal Health, Alaris Products. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2005-12-23.
- Submission: K052790
- Applicant / Sponsor: Cardinal Health, Alaris Products
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5440
- Decision date: 2005-12-23
Classification & Regulation
This clearance is catalogued under FDA product code LHI and 21 CFR 880.5440, within the General Hospital review panel as a Class II device.