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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 the device name listed in this FDA 510(k) record. The listed applicant is Teleflex, Inc.. It received FDA 510(k) clearance on 2016-06-21 under 510(k) 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. The listed applicant is Teleflex, Inc.. The 510(k) number is K153652.

When did ARROW FlexBlock Continuous Peripheral Nerve Block Catheter Kit/Set receive FDA 510(k) clearance?

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

Who is the listed applicant for ARROW FlexBlock Continuous Peripheral Nerve Block Catheter Kit/Set?

The FDA 510(k) record lists Teleflex, Inc. as the applicant. This does not by itself establish the device manufacturer.

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

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT06604039A Clinical Registry to Demonstrate the Safety and Performance of Teleflex Vascular Access DevicesRECRUITINGNCT06779630Safety and Effectiveness of the Orsiro Mission 48-mm Sirolimus Eluting Coronary Stent System in Subjects With Coronary Artery LesionsRECRUITINGNCT07258290Safety and Clinical Performance of the Freesolve Resorbable Magnesium Scaffold (RMS) System in Subjects With Coronary Artery LesionsRECRUITINGNCT07052721Randomized Study of an Analgesic Device Enabling Local Anesthetic Delivery and Neuromodulation After Shoulder/Foot SurgeryCOMPLETEDNCT07638514Postoperative Analgesia Using a Perineural Catheter Versus a Single Nerve Block in Rearfoot SurgeryNOT_YET_RECRUITINGNCT01856166PIEB-PCEA Versus CEI-PCEA for Labor Analgesia in NulliparousCOMPLETED

Other records listing Teleflex, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K241451Rusch Endotracheal Tubes (Reinforced); Rusch Endotracheal Tubes (Safety Clear); Rusch Endotracheal Tubes (Safety Clear Pediatric)

Related Devices (Code: CAZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K222341Arrow 0.2 Micron Flat Filter, GVSArrow International, LLCK210983BD Epilor SyringeBecton, Dickinson and CompanyK201356Plastic LOR SyringeJiangsu Caina Medical Co.,LtdK202699E-Cath STIM acc. TsuiPAJUNK GmbH MedizintechnologieK190345VPCPAJUNK GmbH MedizintechnologieK161075Arrow Epidural Catheter KitTeleflexmedical, Inc.

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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