Magnolia Medical Technologies Inc

FDA Filings

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

FDA Registration(s)
Registration Number3009976527
FEI Number3009976527
NameMAGNOLIA MEDICAL TECHNOLOGIES, INC.
Owner & OperatorMagnolia Medical Technologies, Inc.
Contact Address200 W Mercer Suite 500
Seattle WA 98119 US
Official Correspondent
  • Gregory J Bullington
  • 1-206-6732500-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address200 W Mercer St. Suite 500
Seattle, WA 98119 US
Establishment TypeDevelop Specifications But Do Not Manufacture At This Facility



FDA Filings

Device
Company
DeviceDate
Magnolia Medical Technologies Inc.
Steripath Micro Blood Collection System2020-10-08
Magnolia Medical Technologies, Inc.
Steripath Gen2 Blood Collection System2020-02-28
MAGNOLIA MEDICAL TECHNOLOGIES, INC.
Steripath Micro2012-12-10
MAGNOLIA MEDICAL TECHNOLOGIES, INC.
Steripath Micro Blood Collection System2012-12-10
MAGNOLIA MEDICAL TECHNOLOGIES, INC.
Steripath Gen 22012-12-10
MAGNOLIA MEDICAL TECHNOLOGIES, INC.
Steripath Gen 2 Blood Collection System2012-12-10
MAGNOLIA MEDICAL TECHNOLOGIES, INC.
Steripath Gen 2 Blood Collection Kit2012-12-10
MAGNOLIA MEDICAL TECHNOLOGIES, INC.
Steripath Blood Collection Kit2012-12-10
MAGNOLIA MEDICAL TECHNOLOGIES, INC.
SteriPath2012-12-10
MAGNOLIA MEDICAL TECHNOLOGIES, INC.
SteriPath Blood Collection System2012-12-10
MAGNOLIA MEDICAL TECHNOLOGIES, INC.
Initial Specimen Diversion Device2012-12-10

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