Lumedx

FDA Filings

This page includes the latest FDA filings for Lumedx. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

• Registration Number: 3008012314
• FEI Number: 3008012314
• Name: LUMEDX
• Owner & Operator: LUMEDX
• Contact Address: 110 110th AVE NE (Suite 475) ; Bellevue WA 98004 US
• Official Correspondent:
  • Christopher Pearce
  • x-425-8182326-x
• Registration Status: 1
• Initial Importer: Y
• Registration Expiration: 2020-04-25
• Registration Address: 110 110th Ave NE Ste 475 ; Bellevue, WA 98004 US
• Establishment Type:
  • Repack or Relabel Medical Device
  • Manufacture Medical Device
  • Develop Specifications But Do Not Manufacture At This Facility

FDA Filings

Device Company	Device	Date
PMN K123466 | DQK LUMEDX	HealthView ECG Manager	2013-03-15
PMN K120514 | LLZ LUMEDX	HealthView CardioPACS	2013-03-15
PMN K123466 LUMEDX	HEALTHVIEW ECG MANAGER	2012-12-20
PMN K120514 LUMEDX	CARDIOPACS	2012-07-05
OUG LUMEDX	Lumedx Import Interfaces	2012-04-23
OUG LUMEDX	Lumedx Hybrid Interfaces	2012-04-23
OUG LUMEDX	Lumedx Export Interfaces	2012-04-23
OUG LUMEDX	Lumedx Client Interfaces	2012-04-23
PMN K041581 | LLZ LUMEDX	COMPACS	2009-09-18

Similar & Related FDA Registered Companies

• LUMEDX CORPORATION