FDA 510(k) Applications Submitted by PEPIN MFG., INC.

FDA 510(k) Number Submission Date Device Name Applicant
K060579 03/06/2006 COMFORT/IO IONTOPHORESIS ELECTRODES PEPIN MFG., INC.
K070807 03/26/2007 CUTANEOUS ELECTROTHERAPY AND RECORDING ELECTRODES; TENS ELECTRODES PEPIN MFG., INC.


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