Hospitech Respiration

FDA Filings

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

FDA Registration(s)

• Registration Number: 3007682555
• FEI Number: 3007682555
• Name: HOSPITECH RESPIRATION
• Owner & Operator: Hospitech Respiration
• Contact Address: 15 Atir Yeda street ; Kfar Saba IL-M HaMerkaz 4464312 IL
• Official Correspondent:
  • Yoram Levy
  • 972-4-6388837-x
• US Agent:
  • Tova Rivnay
  • 512 5354930
  • 512 5356103
  • yoram@qsitemed.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 15 Atir Yeda Street ; Kfar Saba HaMerkaz, 4464312 IL
• Establishment Type:
  • Manufacture Medical Device
  • Develop Specifications But Do Not Manufacture At This Facility

FDA Filings

Device Company	Device	Date
PMN K180991 | BSK HOSPITECH RESPIRATION	AG100S	2018-11-02
PMN K150157 | BTR HOSPITECH RESPIRATION	AnapnoGuard 100	2016-04-14
PMN K150157 | BSK HOSPITECH RESPIRATION	AnapnoGuard 100	2016-04-14
PMN K131099 | JCX HOSPITECH RESPIRATION	MASS	2015-01-25
PMN K122721 | BSK HOSPITECH RESPIRATION	Cuffill	2013-05-08
PMN K122721 | BSK HOSPITECH RESPIRATION	AnapnoGuard Cuffill	2013-05-08
PMN K122721 | BSK HOSPITECH RESPIRATION	AG Cuffill	2013-05-08
KYZ HOSPITECH RESPIRATION	AnapnoGuard MASS	2011-01-29
PMN K093126 | BTP HOSPITECH RESPIRATION	AnapnoGuard ETT	2010-11-05

Similar & Related FDA Registered Companies

• Hospitech Respiration Ltd.