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

Clearance record K093138

MT9000 SERIES ELECTRO-STIMULATOR, MODELS MT9000, MT9002, MT9001, MT9004 AND MT9003 · Shenzhen Dongdixin Technology Co., Ltd. · decided 2010-02-12 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
InTENSity DI9698Drive Devilbiss HealthcareGZJ00092237616697
InTENSity DI2738Drive Devilbiss HealthcareGZJ00092237614150
InTENSity DI2195Drive Devilbiss HealthcareGZJ00092237614167
InTENSity DI4738Drive Devilbiss HealthcareGZJ00092237616680
LG Med SupplyDC6100Drive Devilbiss HealthcareGZJ00092237618783
LG Med SupplyDC5700Drive Devilbiss HealthcareGZJ00092237618776
InTENSity DI8195Drive Devilbiss HealthcareGZJ00092237616703
World Wide MedicalDI3717-WWMDrive Devilbiss HealthcareGZJ00092237618585
World Wide MedicalDI4738-WWMDrive Devilbiss HealthcareGZJ00092237618608
InTENSity 10DI1010Drive Devilbiss HealthcareGZJ00813520011933
LG Med SupplyDC7110Drive Devilbiss HealthcareGZJ00092237618790
Liberty Multi-Mode StimulatorLMS 1000LIBERTY MEDICAL SOLUTIONS, LLCGZJ IPF LIH00860000178303
CreedDI1021Drive Devilbiss HealthcareGZJ00092237618530
AnalgesicDI1019-2Drive Devilbiss HealthcareGZJ00092237614679
Direct SupplyDS-TENS10Drive Devilbiss HealthcareGZJ00092237618691
World Wide MedicalDI1010-WWMDrive Devilbiss HealthcareGZJ00092237618516
Reliable MedicalDI2788Drive Devilbiss HealthcareGZJ00092237616390
LG Med SupplyDC8420Drive Devilbiss HealthcareGZJ00092237613733