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FDA 510(k)

FENESTRATED NERVE BLOCK NEEDLE

K-Number: K113662 · 2012-04-20

ApplicantImd, Inc.
Decision Date2012-04-20
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

FENESTRATED NERVE BLOCK NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Imd, Inc.. It received FDA 510(k) clearance on 2012-04-20 under 510(k) number K113662. 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 FENESTRATED NERVE BLOCK NEEDLE?

FENESTRATED NERVE BLOCK NEEDLE is a medical device that received FDA 510(k) clearance on 2012-04-20. The listed applicant is Imd, Inc.. The 510(k) number is K113662.

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

FENESTRATED NERVE BLOCK NEEDLE received FDA 510(k) clearance on 2012-04-20, under 510(k) number K113662.

Who is the listed applicant for FENESTRATED NERVE BLOCK NEEDLE?

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

What is the FDA product code for FENESTRATED NERVE BLOCK NEEDLE?

The FDA product code for FENESTRATED 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.

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Other records listing Imd, 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.

K865082PROPHY CARE SOLUTIONK864215PROPHY CARE SOLUTIONK863133PROPHY CARE PASTE

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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