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FDA 510(k) Applications Submitted by JOHN M MITCHELL
FDA 510(k) Number
Submission Date
Device Name
Applicant
K121398
05/09/2012
CHARLIE GUIDEWIRE (REGULAR), CHARLIE GUIDEWIRE (STIFF)
GUIDEPATH MEDICAL, INC.
K993142
09/21/1999
ELITE CUSTOM
SOMA BLUE, INC.
K993143
09/21/1999
VITALITY SYSTEM
SOMA BLUE, INC.
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