FDA 510(k) Applications Submitted by RIEMSER ARZNEIMITTEL AG
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K113539 | 11/30/2011 | REVOIS PRO IMPLANT STSYEM | RIEMSER ARZNEIMITTEL AG |
| K120152 | 01/18/2012 | CERASORB PLUS | RIEMSER ARZNEIMITTEL AG |
| K113042 | 10/12/2011 | REVOIS IMPLANT SYSTEM | RIEMSER ARZNEIMITTEL AG |
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