Shenzhen Imdk Medical Technology Co L T D

FDA Filings

This page includes the latest FDA filings for Shenzhen Imdk Medical Technology 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 Number: 3015007456
• FEI Number: 3015007456
• Name: zhang
• Owner & Operator: Shenzhen IMDK Medical Technology Co., Ltd.
• Contact Address: C Zone,10F,Building 16,Yuanshan Industri ; SHENZHEN CN-44 Guangdong 518106 CN
• Official Correspondent:
  • XIA YUAN
  • 086-0755-36637905-x
• US Agent:
  • zhang
  • CTI U.S. Inc.
  • 248 4613673
  • robin.zhang@cti-cert.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: Suite 230, 1455 CTI U.S. Inc.Lincoln Parkway, Atlanta, GA, 30346 ; ATL, GA 30346 US
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
PMN K180419 | KNG zhang [Shenzhen IMDK Medical Technology Co., Ltd.]	Ultrasonic Doppler (Model YM-2T8)	2018-10-13
PMN K173123 | DQA zhang [Shenzhen IMDK Medical Technology Co., Ltd.]	Pulse Oximeter	2018-10-13
PMN K173123 | DQA zhang [Shenzhen IMDK Medical Technology Co., Ltd.]	Pulse Oximeter C101H1	2018-10-13
PMN K173123 | DQA zhang [Shenzhen IMDK Medical Technology Co., Ltd.]	Pulse Oximeter C101B2	2018-10-13
PMN K173123 | DQA zhang [Shenzhen IMDK Medical Technology Co., Ltd.]	Pulse Oximeter C101B1	2018-10-13
PMN K173123 | DQA zhang [Shenzhen IMDK Medical Technology Co., Ltd.]	Pulse Oximeter C101A3	2018-10-13
PMN K173123 | DQA zhang [Shenzhen IMDK Medical Technology Co., Ltd.]	Pulse Oximeter C101A2	2018-10-13
PMN K173123 Shenzhen IMDK Medical Technology Co., Ltd.	Pulse Oximeter	2018-08-13
PMN K180419 Shenzhen IMDK Medical Technology Co., Ltd.	Ultrasonic Doppler (Model YM-2T8)	2018-07-19