Clearance Summary
Arrow Pressure Injectable Midline Catheter received FDA 510(k) clearance under submission number K213855, sponsored by Arrow International, LLC Subsidiary of Teleflex Incorporated. 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 2022-09-02.
- Submission: K213855
- Applicant / Sponsor: Arrow International, LLC Subsidiary of Teleflex Incorporated
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5200
- Decision date: 2022-09-02
Classification & Regulation
This clearance is catalogued under FDA product code PND and 21 CFR 880.5200, within the General Hospital review panel as a Class II device.