ClearanceBrief
Company ยท JP

Nemoto Kyorindo Co., Ltd.

FDA 510(k) clearances and medical device recalls filed under this name, 2005 to 2024. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DXTInjector And Syringe, Angiographic7
IZQInjector, Contrast Medium, Automatic1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Aug 27, 2024K242212Disposable Syringe (Kit); Nemoto Disposable Syringe (Kit)
Nemoto Kyorindo Co., Ltd., JP
DXT
Feb 7, 2018K173450PRESS DUO elite, PRESS DUO elite AG
Nemoto Kyorindo Co., Ltd., JP
DXT
Jun 30, 2014K133189DUAL SHOT ALPHA 7
Nemoto Kyorindo Co., Ltd., JP
DXT
Oct 29, 2010K092896REMPRESS AND ANGIOGRAPHY CONTRAST DELIVERY SYSTEM REMPRESS
Nemoto Kyorindo Co., Ltd., JP
DXT
May 21, 2010K091734SONIC SHOT GX
Nemoto Kyorindo Co., Ltd., JP
IZQ
Dec 19, 2007K071691DUAL SHOT ALPHA
Nemoto Kyorindo Co., Ltd.
DXT
Aug 18, 2006K062168CONTRAST DELIVERY SYSTEM - DUAL SHOT ALPHA
Nemoto Kyorindo Co., Ltd., JP
DXT
Oct 17, 2005K052633DUAL SHOT - CONTRAST DELIVERY SYSTEM
Nemoto Kyorindo Co., Ltd., JP
DXT

Latest recalls

DateFirm and productCodeLinked 510(k)
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