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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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