Kailey Check

FDA Filings

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

FDA Registration(s)
Registration Number9617111
FEI Number3006442872
NameKailey Check
Owner & OperatorAMCOR, LTD.
Contact Address1919 Butterfiled Road --
Mundelein IL 60060 US
Official Correspondent
  • Kailey Check
  • x-847-9184287-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1919 S. Butterfield Rd
Mundelein, IL 60060 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Kailey Check [AMCOR, LTD.]
TYVEK Pouch/Roll with STERRAD Chemical Indicator2013-02-07
Kailey Check [AMCOR, LTD.]
TYVEK Pouch/Roll with STERRAD Chemical Indicator2013-02-07
Kailey Check [AMCOR, LTD.]
TYVEK Pouch/Roll with STERRAD Chemical Indicator2013-02-07
Kailey Check [AMCOR, LTD.]
TYVEK Pouch/Roll with STERRAD Chemical Indicator2013-02-07

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