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FDA 510(k) Applications Submitted by LARISA SHPUNGINA
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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