検索結果
このページでは、よみがながつかないところがあります。https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm
510(k) Premarket Notification - accessdata.fda.gov
A 510(K) is a premarket submission made to FDA to demonstrate that the device to be marketed is as safe and effective, that is, substantially equivalent, ...
https://www.fda.gov/medical-devices/510k-clearances/october-2022-510k-clearances
October 2022 510(K) Clearances - FDA
... 07-OCT-22 Chesterfield MO 63005 510(k) ... SE DECISION MADE: 03-OCT-22 Audubon PA 19403 510(k) ... 1 SE DECISION MADE: 07-OCT-22 Gersthofen DE ...
松鼠棋牌510k『wn4.com』w1n2c3o.2022年10月7日22时53分35秒.cj0lslnjyで検索した結果 約2件
