Harbin Quanke Medi Technical Development Co L T D

FDA Filings

This page includes the latest FDA filings for Harbin Quanke Medi Technical Development Co L T D. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3005280264
FEI Number3005280264
NameHARBIN QUANKE MEDI-TECHNICAL DEVELOPMENT CO., LTD.
Owner & OperatorHARBIN QUANKE MEDI-TECHNICAL DEVELOPMENT CO., LTD.
Contact Address42-1 LANE 2, JING WEI STREET DAOLI DISTRICT, HARBIN
HarBin CN-23 Heilongjiang 150010 CN
Official Correspondent
  • XIANGLIN WANG
  • 86-451-84653888-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address42-1 LANE 2, JING WEI STREET DAOLI DISTRICT,
HARBIN Heilongjiang, 150010 CN
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
HARBIN QUANKE MEDI-TECHNICAL DEVELOPMENT CO., LTD.
QK-Therapeutic Apparatus,model:QK-S05,QK-S07,QK-S08,QK-S09.QK-S10,QK-S152015-03-23
HARBIN QUANKE MEDI-TECHNICAL DEVELOPMENT CO., LTD.
QK-Therapeutic Apparatus,model:QK-C01A,QK-C01B,QK-C01CZ,QK-C01EZ.QK-S14.QK-C02FZ,QK-C02D2015-03-23
HARBIN QUANKE MEDI-TECHNICAL DEVELOPMENT CO., LTD.
QK-Therapeutic Apparatus model:QK-C02F,QK-S062015-03-23
HARBIN QUANKE MEDI-TECHNICAL DEVELOPMENT CO., LTD.
QK-SYSTEMIC THERAPEUTIC APPARATUS2015-01-28

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