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

Clearance record K122944

GEMORE TRUE SINE INTERFERENTIAL STIMULATOR · Gemore Technology Co, Ltd. · decided 2012-12-21 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
GEM-STIMGM3A00IFGEMORE TECHNOLOGY CO., LTD.LIH04712832961409
GEM-STIMGM3A20IFGEMORE TECHNOLOGY CO., LTD.LIH04712832960471
GEM-STIMGM3A50IFGEMORE TECHNOLOGY CO., LTD.LIH04712832961423
GEM-STIMGM3A10IFGEMORE TECHNOLOGY CO., LTD.LIH04712832961416