FDA 510(k) Applications Submitted by RITM OKB ZAO
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K131513 | 05/28/2013 | SCENAR (SCELAP, ENISAR, IPENS) CUTANEOUS ELECTRODE FAMILY | RITM OKB ZAO |
| K092117 | 07/14/2009 | SCENAR, MODEL 10 | RITM OKB ZAO |
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