Midwest Medical Mfg

FDA Filings

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

FDA Registration(s)
Registration Number3007589160
FEI Number3007589160
NameMidwest Medical Mfg
Owner & OperatorMIDWEST MEDICAL MFG
Contact Address806 west road
Mountain Home AR 72653 US
Official Correspondent
  • kevin A hurst
  • x-314-6074848-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address806 West Rd
Mountain Home, AR 72653 US
Establishment Type
  • Manufacture Medical Device
  • Manufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device
Company
DeviceDate
Midwest Medical Mfg
asico2013-07-02
Midwest Medical Mfg
Katalyst2009-05-03
Midwest Medical Mfg
Asico2009-05-03
Midwest Medical Mfg
Katalyst2009-05-03
Midwest Medical Mfg
Asico2009-05-03
Midwest Medical Mfg
Karalyst2009-05-03
Midwest Medical Mfg
Asico2009-05-03

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