David Cromwick

FDA Filings

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

FDA Registration(s)
Registration Number3005181518
FEI Number3005181518
NameDavid Cromwick
Owner & OperatorHain Lifescience GmbH
Contact AddressHardwiesenstr. 1
Nehren DE-BW Baden-Wurttemberg 72147 DE
Official Correspondent
  • Gerti Boos
  • 49-747-3945172-0
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address40 Manning Road
Billerica, MA 01821 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
David Cromwick [Hain Lifescience GmbH]
GXT Blood 500 Extraction Kit VER 1.02019-02-15
David Cromwick [Hain Lifescience GmbH]
Arrow Blood DNA 5002019-02-15
David Cromwick [Hain Lifescience GmbH]
NorDiag Arrow2019-02-15
David Cromwick [Hain Lifescience GmbH]
GenoXtract2019-02-15

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