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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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