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FDA 510(k)

Nix Ultra Lice Treatment Kit

K-Number: K163401 · 2017-03-21

ApplicantMedtech Products, Inc.
Decision Date2017-03-21
Product CodeLJL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Nix Ultra Lice Treatment Kit is the device name listed in this FDA 510(k) record. The listed applicant is Medtech Products, Inc.. It received FDA 510(k) clearance on 2017-03-21 under 510(k) number K163401. The device is classified under product code LJL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Nix Ultra Lice Treatment Kit?

Nix Ultra Lice Treatment Kit is a medical device that received FDA 510(k) clearance on 2017-03-21. The listed applicant is Medtech Products, Inc.. The 510(k) number is K163401.

When did Nix Ultra Lice Treatment Kit receive FDA 510(k) clearance?

Nix Ultra Lice Treatment Kit received FDA 510(k) clearance on 2017-03-21, under 510(k) number K163401.

Who is the listed applicant for Nix Ultra Lice Treatment Kit?

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

What is the FDA product code for Nix Ultra Lice Treatment Kit?

The FDA product code for Nix Ultra Lice Treatment Kit is LJL.

Other records listing Medtech Products, Inc. as applicant

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Related Devices (Code: LJL)

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.

K151562Resultz Lice & Egg Removal KitPiedmont Pharmaceuticals, LLC

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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