Weifang Km Electronics Co L T D

FDA Filings

This page includes the latest FDA filings for Weifang Km Electronics 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 Number3010273372
FEI Number3010273372
NameQihui Zhang
Owner & OperatorWeifang KM Electronics Co., LTD
Contact AddressNo. 7999 Health East Street, High-Tech D
Weifang CN-37 Shandong 261000 CN
Official Correspondent
  • Andy PANG
  • 86-136-06464486-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1337 Massachusetts Avenue #158 Arlington
MA, MA 02476 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Qihui Zhang [Weifang KM Electronics Co., LTD]
Diode Laser Treatment System KM200D, KM300D, KM600D, KM800D, KM900D2019-05-09
Weifang KM Electronics Co., LTD
Diode Laser Treatment System2019-04-15

Related Finance Registrations
U.S. Import Records [external site]
Import IDShipmentCargo DescriptionQuantity
2020071360288Puerto Manzanillo,Panama -> San Juan, Puerto RicoSECURITY INSPECTION GATE9 BOX
2020070641090Puerto Manzanillo,Panama -> San Juan, Puerto RicoSECURITY INSPECTION GATE13 BOX
2020070641090Puerto Manzanillo,Panama -> San Juan, Puerto RicoSECURITY INSPECTION GATE13 BOX
202006154586Shanghai ,China (Mainland) -> Miami, FloridaINTELLIGENT ATTENDANCE EQUIPMENT TD6001 PKG

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