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FDA 510(k)

CONTINUOUS PERIPHERAL NERVE BLOCK CATHETER KIT AND SET

K-Number: K121403 · 2012-06-20

ApplicantTeleflex, Inc.
Decision Date2012-06-20
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CONTINUOUS PERIPHERAL NERVE BLOCK CATHETER KIT AND 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 2012-06-20 under 510(k) number K121403. 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 CONTINUOUS PERIPHERAL NERVE BLOCK CATHETER KIT AND SET?

CONTINUOUS PERIPHERAL NERVE BLOCK CATHETER KIT AND SET is a medical device that received FDA 510(k) clearance on 2012-06-20. The listed applicant is Teleflex, Inc.. The 510(k) number is K121403.

When did CONTINUOUS PERIPHERAL NERVE BLOCK CATHETER KIT AND SET receive FDA 510(k) clearance?

CONTINUOUS PERIPHERAL NERVE BLOCK CATHETER KIT AND SET received FDA 510(k) clearance on 2012-06-20, under 510(k) number K121403.

Who is the listed applicant for CONTINUOUS PERIPHERAL NERVE BLOCK CATHETER KIT AND 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 CONTINUOUS PERIPHERAL NERVE BLOCK CATHETER KIT AND SET?

The FDA product code for CONTINUOUS PERIPHERAL NERVE BLOCK CATHETER KIT AND SET is CAZ.

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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.

K153652ARROW FlexBlock Continuous Peripheral Nerve Block Catheter Kit/SetK123974PERCUTANEOUS INTRODUCER KITK103658FLEXTIP PLUS CLOSED TIP EPIDURAL CATHERTERK861951MODIFIED TELEFLEX MEDICAL INTRODUCER CATHETERK860307PEEL AWAY & SPLIT SHEATH PERCU CATH INTRODUCER SET

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

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

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