FDA 510(k), K162784, Silk'n HST

FDA 510(k), K162784, Silk'n HST

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510(K) Number: K162784
Device Name: Silk'n HST
Manufacturer: Home Skinovations Ltd.
Device Classification Name: Light Based Over The Counter Wrinkle Reduction
Regulation Number: 878.4810
Classification Product Code: OHS
Date Received: 10/03/2016
Decision Date: 03/25/2017
Regulation Medical Specialty: General & Plastic Surgery

Total pages: 2549
Fully redacted pages: 2362
Content pages: 187

PLEASE NOTE: Most 510(k)s obtained through FOIA are heavily redacted, often omitting sections related to testing, software, manufacturing, and other technical data. Please be sure to review the total pages, redacted pages, and content pages listed in the description to get a sense of how much of the document is redacted. As the FDA FOIA office explains: “We HEAVILY REDACT the majority of the following portions of 510(k) filings: testing data, technical data, lab reports, manufacturing information, vendor information, substantive discussions regarding deficiencies or additional information requests, internal FDA communications, software and risk analysis, specifications, SOPs, unpublished studies, draft manuals, etc.” If you’d like more details about a specific document before purchasing, please contact us at info@foiadocs.com.

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