Ivwatch L L C

FDA Filings

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

FDA Registration(s)
Registration Number3011490091
FEI Number3011490091
NameIVWATCH, LLC
Owner & OperatorivWatch, LLC
Contact Address700 Tech Center Parkway, Suite 300
Newport News VA 23606 US
Official Correspondent
  • Linda Warren
  • 001-855-4892824-7021
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address700 Tech Center Parkway, Suite 300
Newport News, VA 23606 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
IVWATCH, LLC
ivWatch SmartTouch Sensor 008140880205972020-07-27
IVWATCH, LLC
ivWatch Extension Module 008140880201222020-07-27
IVWATCH, LLC
ivWatch Patient Cable 008140880201152020-07-27
IvWatch, LLC
IvWatch Model 400, Device Accessories: Extension Module, SmartTouch Sensor, Patient Cable2020-07-02
IVWATCH, LLC
ivWatch Patient Monitor 008140880203822019-07-25
IVWATCH, LLC
ivWatch Patient Monitor 008140880200922019-07-25
IVWATCH, LLC
ivWatch Sensor Cable 2019-07-25
IVWATCH, LLC
ivWatch Sensor Receptacle 2019-07-25
IVWATCH, LLC
ivWatch Patient Monitor 008140880200092019-07-25
IVWATCH, LLC
ivWatch Model 4002017-01-13
IvWatch, LLC
IvWatch2016-12-22
IVWATCH, LLC
ivWatch Model 4002016-07-14
IvWatch, LLC
IvWatch Model 4002016-02-11
IVWATCH, LLC
ivWatch Model 4002015-03-03
IvWatch, LLC
IvWatch Model 4002015-02-13

Related Finance Registrations

© 2020 FDA.report
This site is not affiliated with or endorsed by the FDA.