? ? 8月29日，F(xiàn)DA官方網(wǎng)站公布2018年財(cái)年醫(yī)療器械評(píng)審*新收費(fèi)情況。此收費(fèi)將從今年（2017年）10月1日開始實(shí)施，到2018年9月30日截止。

1．其中，*具關(guān)注的FDA 510k 的標(biāo)準(zhǔn)收費(fèi)從USD4690 漲價(jià)到10542 USD；

2．FDA 510k類中小企業(yè)收費(fèi)仍然為USD2636；

詳情可見此：FY 2018 Medical Device User Fee Small Business Qualification and Certification Guidance for Industry, Food and Drug Administration Staff and Foreign Governments (PDF 797KB)

3．工廠注冊(cè)（2018年度）費(fèi)用漲到USD4631。

?For small businesses with an approved SBD.

??Note: all types of 510(k)s (Traditional, Abbreviated, and Special) are subject to the user fee. However, there is no user fee for 510(k)s submitted to the FDA on behalf of an FDA-accredited third-party reviewer.

Small businesses with an approved SBD with gross receipts or sales of $30 million or less are eligible to have the fee waived on their first PMA, PDP, PMR, or BLA.

Annual Establishment Registration Fee: $4,631

?

? There are no waivers or reductions for small establishments, businesses, or groups – all establishments must pay the establishment registration fee.

全文詳情可見FDA官方網(wǎng)站：FY 2018 MDUFA User Fees

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