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FDA 510(k), K172791, Lumilisse IPL Hair Remover
FDA 510(k), K172791, Lumilisse IPL Hair Remover
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510(K) Number: K172791
Device Name: Lumilisse IPL Hair Remover
Manufacturer: Conair Corporation
Device Classification Name: light based over-the-counter hair removal
Regulation Number: 878.4810
Classification Product Code: OHT
Date Received: 09/15/2017
Decision Date: 01/18/2018
Regulation Medical Specialty: General & Plastic Surgery
Device Name: Lumilisse IPL Hair Remover
Manufacturer: Conair Corporation
Device Classification Name: light based over-the-counter hair removal
Regulation Number: 878.4810
Classification Product Code: OHT
Date Received: 09/15/2017
Decision Date: 01/18/2018
Regulation Medical Specialty: General & Plastic Surgery
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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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