Clearance Summary
ULTRAQUIK PERIPHERAL NERVE BLOCK NEEDLE received FDA 510(k) clearance under submission number K122690, sponsored by Arrow International, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2012-12-21.
- Submission: K122690
- Applicant / Sponsor: Arrow International, Inc.
- Clearance pathway: Traditional
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.5140
- Decision date: 2012-12-21
Classification & Regulation
This clearance is catalogued under FDA product code CAZ and 21 CFR 868.5140, within the Anesthesiology review panel as a Class II device.