Clearance Summary
COOK BRACH NEEDLE/RADIO DELIV CATH/FLEXI FLEXICATH received FDA 510(k) clearance under submission number K940550, sponsored by Cook, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1994-08-17.
- Submission: K940550
- Applicant / Sponsor: Cook, Inc.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class I
- Regulation citation: 21 CFR 892.5650
- Decision date: 1994-08-17
Classification & Regulation
This clearance is catalogued under FDA product code IWJ and 21 CFR 892.5650, within the Radiology review panel as a Class I device.