Clearance Summary
CODAN MEDLON BC110 VIAL ADAPTER CODAN SPIKE received FDA 510(k) clearance under submission number K960921, sponsored by Codan Medlon, Inc.. 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 1996-04-17.
- Submission: K960921
- Applicant / Sponsor: Codan Medlon, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5440
- Decision date: 1996-04-17
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.