Midwest Products Engineering

FDA Filings

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

FDA Registration(s)
Registration Number3003500271
FEI Number3003500271
NameMIDWEST PRODUCTS AND ENGINEERING
Owner & OperatorMidwest Products and Engineering
Contact Address10597 Glenbrook Ct
Milwaukee WI 53224 US
Official Correspondent
  • Jim Gartzke
  • 001-414-4344023-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address10597 W Glenbrook Ct
Milwaukee, WI 53224 US
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)



FDA Filings

Device
Company
DeviceDate
MIDWEST PRODUCTS AND ENGINEERING
SCMC12019-02-27
MIDWEST PRODUCTS AND ENGINEERING
SCMC32019-02-27
MIDWEST PRODUCTS AND ENGINEERING
Bassinet Assembly2018-03-14
MIDWEST PRODUCTS AND ENGINEERING
Helix Cart2016-09-07
MIDWEST PRODUCTS AND ENGINEERING
Sterrad Cart2013-01-28

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