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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