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FDA 510(k)

ARROW FLEXBLOCK CONTINUOUS PERIPHERAL NERVE BLOCK CATHETER

K-Number: K122027 · 2012-08-28

ApplicantArrow International, Inc.
Decision Date2012-08-28
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ARROW FLEXBLOCK CONTINUOUS PERIPHERAL NERVE BLOCK CATHETER 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 2012-08-28 under 510(k) number K122027. 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?

ARROW FLEXBLOCK CONTINUOUS PERIPHERAL NERVE BLOCK CATHETER is a medical device that received FDA 510(k) clearance on 2012-08-28. The listed applicant is Arrow International, Inc.. The 510(k) number is K122027.

When did ARROW FLEXBLOCK CONTINUOUS PERIPHERAL NERVE BLOCK CATHETER receive FDA 510(k) clearance?

ARROW FLEXBLOCK CONTINUOUS PERIPHERAL NERVE BLOCK CATHETER received FDA 510(k) clearance on 2012-08-28, under 510(k) number K122027.

Who is the listed applicant for ARROW FLEXBLOCK CONTINUOUS PERIPHERAL NERVE BLOCK CATHETER?

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 ARROW FLEXBLOCK CONTINUOUS PERIPHERAL NERVE BLOCK CATHETER?

The FDA product code for ARROW FLEXBLOCK CONTINUOUS PERIPHERAL NERVE BLOCK CATHETER is CAZ.

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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.

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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.

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