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FDA 510(k), K163401, Nix Ultra Lice Treatment Kit
FDA 510(k), K163401, Nix Ultra Lice Treatment Kit
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510(K) Number: K163401
Device Name: Nix Ultra Lice Treatment Kit
Manufacturer: MEDTECH PRODUCTS INC.
Device Classification Name: detectors and removers, lice, (including combs)
Regulation Number: 880.5960
Classification Product Code: LJL
Date Received: 12/05/2016
Decision Date: 03/21/2017
Regulation Medical Specialty: General Hospital
Device Name: Nix Ultra Lice Treatment Kit
Manufacturer: MEDTECH PRODUCTS INC.
Device Classification Name: detectors and removers, lice, (including combs)
Regulation Number: 880.5960
Classification Product Code: LJL
Date Received: 12/05/2016
Decision Date: 03/21/2017
Regulation Medical Specialty: General Hospital
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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