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FDA 510(k)

ARROW FlexBlock Continuous Peripheral Nerve Block Catheter Kit/Set

K-Number: K153652 · 2016-06-21

ApplicantTeleflex, Inc.
Decision Date2016-06-21
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ARROW FlexBlock Continuous Peripheral Nerve Block Catheter Kit/Set is a medical device manufactured by Teleflex, Inc.. It received FDA 510(k) clearance on 2016-06-21 under approval number K153652. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARROW FlexBlock Continuous Peripheral Nerve Block Catheter Kit/Set?

ARROW FlexBlock Continuous Peripheral Nerve Block Catheter Kit/Set is a medical device that received FDA 510(k) clearance on 2016-06-21. It is manufactured by Teleflex, Inc.. The 510(k) number is K153652.

When was ARROW FlexBlock Continuous Peripheral Nerve Block Catheter Kit/Set approved by the FDA?

ARROW FlexBlock Continuous Peripheral Nerve Block Catheter Kit/Set received FDA 510(k) clearance on 2016-06-21, under approval number K153652.

What company makes ARROW FlexBlock Continuous Peripheral Nerve Block Catheter Kit/Set?

ARROW FlexBlock Continuous Peripheral Nerve Block Catheter Kit/Set is manufactured by Teleflex, Inc..

What is the FDA product code for ARROW FlexBlock Continuous Peripheral Nerve Block Catheter Kit/Set?

The FDA product code for ARROW FlexBlock Continuous Peripheral Nerve Block Catheter Kit/Set is CAZ.

Related Clinical Trials

NCT07222787 Post-market Safety and Effectiveness of the CORUS-LX System in Improving Lumbar Interbody Fusion Outcomes RECRUITING NCT07613489 Photobiomodulation for Diabetic Peripheral Neuropathy ACTIVE_NOT_RECRUITING NCT06958731 In-plane Versus Real Time Bi-plane Single-operator Laser-assisted With a Innovative T-shaped Probe for Ultrasound-guided Internal Jugular Vein Catheterization:A Randomized Controlled Trial ENROLLING_BY_INVITATION NCT07601763 Pulsed Field Ablation Outcomes With Efficacy and Randomization in Atrial Fibrillation (POWER-AF) RECRUITING NCT04246281 The RESET Clinical Trial: SPRINT® Peripheral Nerve Stimulation for the Treatment of Back Pain COMPLETED NCT06121232 Exploring the Benefit of Neuromodulation in Treating Chemo-induced Peripheral Neuropathy Using Peripheral Neuropathy Markers (Meissner's Corpuscles and Epidermal Nerve Fiber Density) and Sensory Testing (Quantitative Sensory and Gait Testing): A Single Center Feasibility Study ACTIVE_NOT_RECRUITING

Related PubMed Literature

PMID: 41470022 Low-intensity pulsed ultrasound for peripheral nerve regeneration: mechanobiological mechanisms and translational potential. Journal of translational medicine (2025)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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