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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 a medical device manufactured by Medtech Products, Inc.. It received FDA 510(k) clearance on 2017-03-21 under approval 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. It is manufactured by Medtech Products, Inc.. The 510(k) number is K163401.

When was Nix Ultra Lice Treatment Kit approved by the FDA?

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

What company makes Nix Ultra Lice Treatment Kit?

Nix Ultra Lice Treatment Kit is manufactured by Medtech Products, Inc..

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

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

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Other Devices by Medtech Products, Inc.

K161294Compound W Wart Removal System Dual Power K172373Compound W Nitro-Freeze K180933DenTek Ultimate Dental Guard K202974DenTek Fresh Protect Dental Guard K242803Compound W Skin Tag Remover

Related Devices (Code: LJL)

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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