FDA 510(k) Applications Submitted by MICHELLE SAWYER

FDA 510(k) Number Submission Date Device Name Applicant
K030708 03/06/2003 SLENDERTONE FLEX ABDOMINAL TRAINING SYSTEM, TYPE 515 BIO-MEDICAL RESEARCH, LTD.
K023913 11/25/2002 NEUROTECH BAXOLVE TYPE 294 BIO-MEDICAL RESEARCH, LTD.
K023916 11/25/2002 BMR NEUROTECH BACK TENS AND LUMBAR SUPPORT DEVICE. TYPE 294 BIO-MEDICAL RESEARCH, LTD.
K014019 12/06/2001 NEUROTECH MEDISTIM PLUS, TYPE 291 BIO-MEDICAL RESEARCH, LTD.
K014020 12/06/2001 NT MEDITENS PLUS, TYPE 290 BIO-MEDICAL RESEARCH, LTD.


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