联系电话:0755-23202750

2019年医疗类产品FDA收费标准

FDA于美国当地时间201881日公布了2019财年(2018101–2019930)FDA各项服务的收费案,2018年内731FDA更正了部分收费金额。 

  

FDA2019财年费率比2018财年有略微的提高。 

FDA公司年度认证费用由原来的USD4,624提升到USD4,884,提高了5.7%  

FDA510K审核费标准费率由原来的USD1,0566提高到USD10,953,提高了USD387 

  

Important Information on Medical Device User Fees for Fiscal Year 2019

(适用于FDA 2019财年:2018101日至2019930) 

  

主要费率: 

项目 

2019财年(2018.10.01-2019.09.30) 

2019财年医疗器械公司注册年度认证费 

USD4,884个制造商(无减免) 

2019财年FDA510(K)审核费(每个510K申请) 

USD10,953 (标准收费) 

USD 2,738 (FDA认证为小企业资质的公司享受该优惠收费) 

* FDA小企业资质指的是公司最近税收年度的总收入或销售额未超过1亿美金,并需要提前1-2个月申请FDA小企业资质认证后才能享受优惠; 

Small Business: This is defined as having gross receipts or sales of no more than $100 million for the most recent tax year.  

     

其他费率: 

FY201 9User Fees for Medical Device Applications
The following table identifies the FY18 User Fees for Applications (in US Dollars) 


Application Type

Standard Fee

Small Business Fee?

510(k)?

10,953

2,738

513(g)

4,349

2,175

PMA, PDP, PMR, BLA

322,147

80,537

De Novo classification request

96,644

24,161

panel-track supplement

241,610

60,403

180-day supplement

48,322

12,081

real-time supplement

22,550

5,638

BLA efficacy supplement

322,147

80,537

annual report

11,275

2,819

30-day notice

5,154

2,577


?  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 by an FDA-accredited third-party reviewer. 

  

ZCQC将从201810月开始为客人进行2019年度认证和受理新认证申请。 

  

24小时热线:15602970173 

邮件咨询:info@zcqc.org 

联络QQ: 2695669655