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FDA 510(k) Applications Submitted by BIONICARE MEDICAL TECHNOLOGIES, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K030332
01/31/2003
MODIFICATION TO BIONICARE STIMULATOR SYSTEM, MODEL BIO-1000
BIONICARE MEDICAL TECHNOLOGIES, INC.
K052625
09/23/2005
BIONICARE STIMULATOR SYSTEM, MODEL BIO-1000
BIONICARE MEDICAL TECHNOLOGIES, INC.
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