Nemoto Kyorindo Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Disposable Syringe (Kit), PRESS DUO elite, PRESS DUO elite AG
8
Total
8
Cleared
0
Denied
FDA 510(k) Regulatory Record - Nemoto Kyorindo Co., Ltd. Cardiovascular ✕
6 devices
Cleared
Feb 07, 2018
PRESS DUO elite, PRESS DUO elite AG
Cardiovascular
93d
Cleared
Jun 30, 2014
DUAL SHOT ALPHA 7
Cardiovascular
256d
Cleared
Oct 29, 2010
REMPRESS AND ANGIOGRAPHY CONTRAST DELIVERY SYSTEM REMPRESS
Cardiovascular
403d
Cleared
Dec 19, 2007
DUAL SHOT ALPHA
Cardiovascular
182d
Cleared
Aug 18, 2006
CONTRAST DELIVERY SYSTEM - DUAL SHOT ALPHA
Cardiovascular
18d
Cleared
Oct 17, 2005
DUAL SHOT - CONTRAST DELIVERY SYSTEM
Cardiovascular
21d