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FDA 510(k) Applications Submitted by PETER SULLIVAN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K030039
01/06/2003
PATHWAY STM-10 PELVIC FLOOR STIMULATOR
THE PROMETHEUS GROUP
K960761
02/26/1996
PATHWAY ELECTROMYOGRAPH MODEL TR-10 & TR-20
THE PROMETHEUS GROUP
K973537
09/18/1997
PATHWAY ELECTROMYOGRAPH
THE PROMETHEUS GROUP
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