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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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