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FDA 510(k)

Resultz Lice & Egg Removal Kit

K-Number: K151562 · 2017-05-08

Decision Date2017-05-08
Product CodeLJL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Resultz Lice & Egg Removal Kit is the device name listed in this FDA 510(k) record. The listed applicant is Piedmont Pharmaceuticals, LLC. It received FDA 510(k) clearance on 2017-05-08 under 510(k) number K151562. 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 Resultz Lice & Egg Removal Kit?

Resultz Lice & Egg Removal Kit is a medical device that received FDA 510(k) clearance on 2017-05-08. The listed applicant is Piedmont Pharmaceuticals, LLC. The 510(k) number is K151562.

When did Resultz Lice & Egg Removal Kit receive FDA 510(k) clearance?

Resultz Lice & Egg Removal Kit received FDA 510(k) clearance on 2017-05-08, under 510(k) number K151562.

Who is the listed applicant for Resultz Lice & Egg Removal Kit?

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

What is the FDA product code for Resultz Lice & Egg Removal Kit?

The FDA product code for Resultz Lice & Egg Removal Kit is LJL.

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.