FDA 510(k) Applications Submitted by Accelerated Care Plus

FDA 510(k) Number Submission Date Device Name Applicant
K093600 11/20/2009 OMNISTIM CONTINENCE+ PELVIC FLOOR STIMULATION SYSTEM ACCELERATED CARE PLUS
K153456 12/01/2015 Megapulse III Shortwave Diathermy Accelerated Care Plus


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