Allergan Botox Needle Electrode
K-Number: K173815 · 2018-06-29
Device Summary
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. The listed applicant is Natus Manufacturing Limited. The 510(k) number is K173815.
When did Allergan Botox Needle Electrode receive FDA 510(k) clearance?
Allergan Botox Needle Electrode received FDA 510(k) clearance on 2018-06-29, under 510(k) number K173815.
Who is the listed applicant for Allergan Botox Needle Electrode?
The FDA 510(k) record lists Natus Manufacturing Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Allergan Botox Needle Electrode?
The FDA product code for Allergan Botox Needle Electrode is IKT.
Other records listing Natus Manufacturing Limited 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.
Related Devices (Code: IKT)
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.
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.