FDA 510(k) Applications Submitted by KENT HOFFMAN

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.
K971437 04/18/1997 BIONICARE STIMULATOR SYSTEM. MODEL BIO-1000 MURRAY ELECTRONICS
K983228 09/15/1998 BIONICARE STIMILATOR SYSTEM, MODEL BIO-1000 MURRAY ELECTRONICS


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