加拿大外贸
最近谈了一个客户，货物到美国了现在客户告知我们需要做FDA注册，我们已经按照客户要求去做注册，但是现在有要求先申请510K评审，有没有大神了解510K的。评论
510（k)文件通常包含哪些内容：
Medical Device User Fee Cover Sheet
CDRH Premarket Review Submission Cover Sheet
Certification of Compliance with ClinicalTrials.gov Data Bank
Cover letter as described in the format guidance
Table of Contents (recommended)
Indications for Use. See Determination of Intended Use for 510(k) Devices (Update to K98-1) for additional information on indications for use.
510(k) Summary (21 CFR 807.92) or 510(k) Statement (21 CFR 807.93)
Standards Data Report for 510(K)s.
Truthful and Accuracy Statement (21 CFR 807.87(k))
Class III Certification and Summary for Class III devices (21 CFR 807.94)
Items required under 21 CFR 807.87 (Information required in a Premarket Notification submission), including
the name of device, include the trade or proprietary name, if any, and the common or usual name or classification name of the device. Provide what you believe to be the classification of the device, approprate panel (e.g. cardiovascular, dental, etc.), and product code, if known.
description of the device, include device specifications and reference applicable guidance documents, special controls, or standards; photographs or engineering drawings should be supplied, if applicable
comparison with a predicate device(s), indicating similarities and/or differences accompanied by data, as appropriate; this information may include an identification of materials, design considerations, energy expected to be used or delivered by the device, and a description of the operational principles of the device.
intended use of the device,
proposed label, labeling, and advertisements for the device and directions for use.
Information on sterilization, biocompatibility, expiration date, etc., if applicable.
评论
可以的楼主，看你那边是什么产品的FDA 做510K应该是属于医疗类的了，属于医疗类的费用比较高，如果您有这方面的问题也可以看下我的资料联系我，有什么问题问我就好，能合作当然更好
评论
是什么产品 申请510K需要在国内测试 而且也需要先申请FDA
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