Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ULTRAQUIK PERIPHERAL NERVE BLOCK NEEDLE

K-Number: K122690 · 2012-12-21

ApplicantArrow International, Inc.
Decision Date2012-12-21
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ULTRAQUIK PERIPHERAL NERVE BLOCK NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Arrow International, Inc.. It received FDA 510(k) clearance on 2012-12-21 under 510(k) number K122690. 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 ULTRAQUIK PERIPHERAL NERVE BLOCK NEEDLE?

ULTRAQUIK PERIPHERAL NERVE BLOCK NEEDLE is a medical device that received FDA 510(k) clearance on 2012-12-21. The listed applicant is Arrow International, Inc.. The 510(k) number is K122690.

When did ULTRAQUIK PERIPHERAL NERVE BLOCK NEEDLE receive FDA 510(k) clearance?

ULTRAQUIK PERIPHERAL NERVE BLOCK NEEDLE received FDA 510(k) clearance on 2012-12-21, under 510(k) number K122690.

Who is the listed applicant for ULTRAQUIK PERIPHERAL NERVE BLOCK NEEDLE?

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

What is the FDA product code for ULTRAQUIK PERIPHERAL NERVE BLOCK NEEDLE?

The FDA product code for ULTRAQUIK PERIPHERAL NERVE BLOCK NEEDLE 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Arrow International, 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.

K201112AC3 IABP, AC3 Optimus IABP, AutoCAT2 Wave IABP, AutoCAT2 IABPK200634Arrow FiberOptix Intra-Aortic Balloon Catheter KitK190101UltraFlex IABK190117Fiberoptix IABK162820AC3 Series IABP SystemK130192NEXTSTEP RETROGRADE

View all 18 devices →

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.

K261372Profoject™ LOR SyringeCMT Health PTE., Ltd.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 Medizintechnologie

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.

↑