FDA 510(k) Applications Submitted by Nemoto Kyorindo Co., Ltd.

FDA 510(k) Number Submission Date Device Name Applicant
K092896 09/21/2009 REMPRESS AND ANGIOGRAPHY CONTRAST DELIVERY SYSTEM REMPRESS NEMOTO KYORINDO CO., LTD.
K173450 11/06/2017 PRESS DUO elite, PRESS DUO elite AG Nemoto Kyorindo Co., Ltd.
K133189 10/17/2013 DUAL SHOT ALPHA 7 NEMOTO KYORINDO CO., LTD.
K091734 06/11/2009 SONIC SHOT GX NEMOTO KYORINDO CO., LTD.
K071691 06/20/2007 DUAL SHOT ALPHA NEMOTO KYORINDO CO., LTD.
K062168 07/31/2006 CONTRAST DELIVERY SYSTEM - DUAL SHOT ALPHA NEMOTO KYORINDO CO., LTD.
K052633 09/26/2005 DUAL SHOT - CONTRAST DELIVERY SYSTEM NEMOTO KYORINDO CO., LTD.


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