FDA 510(k) Applications Submitted by JIM KNIPFER
| 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. |
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