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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K113010

FDES100(TENS AND EMS STIMULATOR, FDES102(ED402) TENS STIMULATOR · Famidoc Technology Co., Ltd. · decided 2012-12-21 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
FamidocFDES101Famidoc Technology Co.,Ltd.GZJ IPF06970389634018
FamidocFDES108AFamidoc Technology Co.,Ltd.GZJ IPF06970389630102
GRAFCOGF-DF5GF HEALTH PRODUCTS, INC.GZJM368GFDF51
FamidocFDES102Famidoc Technology Co.,Ltd.GZJ06970389634025
FamidocFDES116AFamidoc Technology Co.,Ltd.GZJ IPF06970389630096
FamidocFDES103Famidoc Technology Co.,Ltd.GZJ06970389634032
acculoveFDES108Famidoc Technology Co.,Ltd.GZJ IPF00818218024813
FamidocFDES100Famidoc Technology Co.,Ltd.GZJ06970389634001
acculoveFDES116Famidoc Technology Co.,Ltd.GZJ IPF00818218024806