Nemoto Kyorindo Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K242212 | Disposable Syringe (Kit); Nemoto Disposable Syringe (Kit) | August 27, 2024 |
| K173450 | PRESS DUO elite, PRESS DUO elite AG | February 7, 2018 |
| K133189 | DUAL SHOT ALPHA 7 | June 30, 2014 |
| K092896 | REMPRESS AND ANGIOGRAPHY CONTRAST DELIVERY SYSTEM REMPRESS | October 29, 2010 |
| K091734 | SONIC SHOT GX | May 21, 2010 |
| K071691 | DUAL SHOT ALPHA | December 19, 2007 |
| K062168 | CONTRAST DELIVERY SYSTEM - DUAL SHOT ALPHA | August 18, 2006 |
| K052633 | DUAL SHOT - CONTRAST DELIVERY SYSTEM | October 17, 2005 |