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

Clearance record K123711

PATIENT MONITOR · Shenzhen Creative Industry Co., Ltd. · decided 2013-10-01 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Patient MonitorPC-3000Shenzhen Creative Industry Co., Ltd.CCK DQA DXN MWI06941900604285
TotalVitalsN/AGlobalmed Holdings, LLCDQAB377GMDTVSBPO2T0