FDA 510(k) Applications Submitted by SALUMEDICA, L.L.C.

FDA 510(k) Number Submission Date Device Name Applicant
K100382 02/16/2010 SALUTUNNEL NERVE PROTECTOR, MODEL ED-20329, ED-20330, ED-20331 SALUMEDICA, L.L.C.
K002098 07/11/2000 SALUMEDICA NERVE CUFF SALUMEDICA, L.L.C.


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