FDA 510(k) Applications Submitted by NORDION INTERNATIONAL, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K963497 | 09/03/1996 | GAMMACELL 3000 ELAN, VERSION 1.0 AND GAMMACELL 1000 ELITE, VERSION 1.0 | NORDION INTERNATIONAL, INC. |
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