Donna Connolly

FDA Filings

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

FDA Registration(s)
Registration Number9680933
FEI Number1000637007
NameDonna Connolly
Owner & OperatorDELTEX MEDICAL LIMITED
Contact AddressTERMINUS ROAD
CHICHESTER GB-WSX West Sussex PO19 8TX GB
Official Correspondent
  • Graham Lowe
  • 44-1243-774-837
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressDeltex Medical SC, Inc. 330 E. Coffee Street
Greenville, SC 29601 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Donna Connolly [DELTEX MEDICAL LIMITED]
HD-ICG Hub2018-11-29
Donna Connolly [DELTEX MEDICAL LIMITED]
KDP72 Doppler Probe2015-12-17
Donna Connolly [DELTEX MEDICAL LIMITED]
CardioQ-EDM+ Cardiac Function and Fluid Status Monitoring System2013-11-11
Donna Connolly [DELTEX MEDICAL LIMITED]
CardioQ-EDM Cardiac Function and Fluid Status Monitoring Sys2011-11-04
Donna Connolly [DELTEX MEDICAL LIMITED]
CardioQ-EDM Cardiac Function and Fluid Status Monitoring Sys2011-11-04
Donna Connolly [DELTEX MEDICAL LIMITED]
CardioQ-EDM Cardiac Function and Fluid Status Monitoring Sys2011-11-04
Donna Connolly [DELTEX MEDICAL LIMITED]
I2S Doppler Probe (6 hour)2009-10-06
Donna Connolly [DELTEX MEDICAL LIMITED]
I2P Doppler Probe (24 hour)2009-10-06
Donna Connolly [DELTEX MEDICAL LIMITED]
I2C Doppler Probe (72 hour)2009-10-06
Donna Connolly [DELTEX MEDICAL LIMITED]
DP240 (9070-7006)2007-12-07
Donna Connolly [DELTEX MEDICAL LIMITED]
CardioQ Cardiac Output and Fluid Status Monitoring System2007-12-07
Donna Connolly [DELTEX MEDICAL LIMITED]
CardioQ Cardiac Output and Fluid Status Monitoring System2007-12-07
Donna Connolly [DELTEX MEDICAL LIMITED]
CardioQ Cardiac Output and Fluid Status Monitoring System2007-12-07
Donna Connolly [DELTEX MEDICAL LIMITED]
CardioQ & CardioQ-EDM Roll Stand2005-04-04

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