FDA 510(k), K191828, Vathin Video Bronchoscope System

FDA 510(k), K191828, Vathin Video Bronchoscope System

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510(K) Number: K191828
Device Name: Vathin Video Bronchoscope System
Manufacturer: Hunan Vathin Medical Instrument Co., Ltd.
Device Classification Name: bronchoscope (flexible or rigid)
Regulation Number: 874.4680
Classification Product Code: EOQ
Date Received: 07/08/2019
Decision Date: 02/13/2020
Regulation Medical Specialty: Ear Nose & Throat

Total pages: 1,009
Fully redacted pages: 837
Content pages: 172

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or additional information requests, internal FDA communications, software and risk analysis, specifications, SOPs, unpublished studies, draft manuals, etc.”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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