FDA 510(k) Applications Submitted by BODEN S LAI

FDA 510(k) Number Submission Date Device Name Applicant
K091833 06/22/2009 GEM-STONE ABDOMINAL TRAINING SYSTEM; MODEL GEM-TONE 310PE/320PE/330PE/340PE/350PE. GEMORE TECHNOLOGY CO., LTD.
K102926 10/04/2010 GEMORE MUSCLE CONDITIONER; GEMORE TECHNOLOGY CO., LTD.
K060222 01/30/2006 LOW BACK PAIN RELIEF SYSTEM /MODELS GM310PP,GM320PP,GM321PP, AND GM330PP GEMORE TECHNOLOGY CO., LTD.
K122944 09/24/2012 GEMORE TRUE SINE INTERFERENTIAL STIMULATOR GEMORE TECHNOLOGY CO., LTD.
K122948 09/24/2012 GEM-STIM COMBO STIMULATOR GEMORE TECHNOLOGY CO., LTD.
K102933 10/04/2010 GEM-TONE BODY TRAINING SYSTEM GEMORE TECHNOLOGY CO., LTD.
K150681 03/17/2015 GEMORE OTC TENS GEMORE TECHNOLOGY CO., LTD.
K120569 02/27/2012 GEMORE TENS SYSTEM GEMORE TECHNOLOGY CO., LTD.
K032719 09/02/2003 GM3 SERIES IF TENS, MODEL GM3X2IF (WHERE X IS A PARAMETER OF DIFFERENT HOUSING) GEMORE TECHNOLOGY CO., LTD.
K032720 09/02/2003 GEM-STIM TENS, MODELS GM3XY AND GM3AXY GEMORE TECHNOLOGY CO., LTD.
K042559 09/21/2004 GEM-TWIN TENS/ MODELS GM3XY/Z GEMORE TECHNOLOGY CO., LTD.
K032994 09/25/2003 GM3 SERIES HV TENS, MODEL GM3X3HV (WHERE X IS PARAMETER OF DIFFERENT HOUSING) GEMORE TECHNOLOGY CO., LTD.


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