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FDA 510(k)

Allergan Botox Needle Electrode

K-Number: K173815 · 2018-06-29

ApplicantNatus Manufacturing Limited
Decision Date2018-06-29
Product CodeIKT
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Allergan Botox Needle Electrode is a medical device manufactured by Natus Manufacturing Limited. It received FDA 510(k) clearance on 2018-06-29 under approval number K173815. The device is classified under product code IKT. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Allergan Botox Needle Electrode?

Allergan Botox Needle Electrode is a medical device that received FDA 510(k) clearance on 2018-06-29. It is manufactured by Natus Manufacturing Limited. The 510(k) number is K173815.

When was Allergan Botox Needle Electrode approved by the FDA?

Allergan Botox Needle Electrode received FDA 510(k) clearance on 2018-06-29, under approval number K173815.

What company makes Allergan Botox Needle Electrode?

Allergan Botox Needle Electrode is manufactured by Natus Manufacturing Limited.

What is the FDA product code for Allergan Botox Needle Electrode?

The FDA product code for Allergan Botox Needle Electrode is IKT.

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Other Devices by Natus Manufacturing Limited

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Related Devices (Code: IKT)

K152984Disposable Concentric Needle electrodes, Disposable Monopolar Needle electrodes, Disposable EP Needle electrodes, Disposable Hypodermic Needle electrodesBio Protech, Inc. K161430Myoject Luer Lock Needle ElectrodeNatus Manufacturing Limited K253581Disposable Concentric Needle Electrode 0.30x25mm Red (TE/B50700-001); Disposable Concentric Needle Electrode 0.40x25mm Yellow (TE/B50700-002); Disposable Concentric Needle Electrode 0.30x30mm Pink (TE/B50700-006); Disposable Concentric Needle Electrode 0.45x37mm Green (TE/B50700-003); Disposable Concentric Needle Electrode 0.45x50mm Blue (TE/B50700-004); Disposable Concentric Needle Electrode 0.60x75mm Violet (TE/B50700-005)Technomed Europe

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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