FDA 510(k) Applications for Medical Device Product Code "GZO"
(Device, Galvanic Skin Response Measurement)

FDA 510(k) Number Applicant Device Name Decision Date
K003480 BIO-SCAN, INC. BIOFIND 05/11/2001
K993824 BIOMERIDIAN, INT. MSAS PROFESSIONAL 01/20/2000
K053004 BIOMERIDIAN, INT. MSAS-VANTAGE 01/13/2006
K032935 EDX EPI-SCAN, INC. EPI-SCAN, MODEL P 100 11/20/2003
K023355 GALLOWAY TECHNOLOGIES, LLC ASYRA 06/24/2003
K993202 GENERAL DEVICES EIM-107 PREP-CHECK 12/17/1999
K100233 IMPETO MEDICAL SUDOSCAN 06/14/2010
K141872 IMPETO MEDICAL INC SUDOSCAN 11/21/2014
K102166 L.D. TECHNOLOGY, LLC ELECTRO INTERSTITIAL SCAN 12/10/2010
K131568 LD TECHNOLOGY LLC SUDO PATH 06/28/2013
K152216 LD TECHNOLOGY LLC SudoC 09/24/2015
K150804 MEDEIA, INC. QBioScan 10/19/2015
K020360 MERIDIAN CO., LTD. ABR-2000 08/29/2002
K001347 MERIDIAN CO., LTD. MERIDIAN-II AND MERDIAN-PLUS 11/03/2000
K010897 MERIDIAN CO., LTD. MERIDIAN-PORTABLE 06/19/2001
K970436 NATURAL HERBAL PRODUCTS, INC. E-READER 08/15/1997
K992129 PHAZX SYSTEMS, INC. PHAZX VLD-100 09/17/1999
K020568 VIBRANT HEALTH AKUPORT M-2 04/30/2002
K020567 VIBRANT HEALTH AKUPORT M1 05/02/2002
K020565 VIBRANT HEALTH EAV COMBI-2 04/30/2002
K020564 VIRBRANT HEALTH EAV KINDLING 2000S GSR DEVICE 04/30/2002
K111308 ZYTO TECHNOLOGIES, INC ZYTO HAND CRADLE 08/30/2011


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