Interrad Medical Inc

FDA Filings

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

FDA Registration(s)
Registration Number3007795799
FEI Number3007795799
NameInterrad Medical Inc
Owner & OperatorInterrad Medical Inc
Contact Address181 Cheshire Lane, Suite 100
Plymouth MN 55441 US
Official Correspondent
  • Joseph Goldberger
  • x-763-2256699-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address181 Cheshire Ln N Ste 100
Minneapolis, MN 55441 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
INTERRAD MEDICAL, INC
SecurAcath 4001802020-06-11
INTERRAD MEDICAL, INC
SecurAcath 4002002020-06-11
INTERRAD MEDICAL, INC
SecurAcath 4001602019-07-22
INTERRAD MEDICAL, INC
SecurAcath 4001202019-07-22
INTERRAD MEDICAL, INC
SecurAcath 4001502019-07-22
INTERRAD MEDICAL, INC
SecurAcath 4001102019-07-22
INTERRAD MEDICAL, INC
SecurAcath 4001402019-07-22
INTERRAD MEDICAL, INC
SecurAcath 4001302019-07-22
Interrad Medical Inc
SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8F2019-07-09
Interrad Medical Inc
SecurAcath2018-12-17
Interrad Medical Inc
SecurAcath2018-12-17
Interrad Medical Inc
SecurAcath2018-06-26
Interrad Medical Inc
SecurAcath2012-10-09
Interrad Medical Inc
SecurAcath2012-10-09
INTERRAD MEDICAL INC
SECURACATH2012-04-27
INTERRAD MEDICAL, INC.
SECURACATH UNIVERSAL2010-07-09
INTERRAD MEDICAL, INC.
MODIFICATION TO SECURACATH, MODEL: SPK012009-03-04
INTERRAD MEDICAL, INC.
SECURACATH CATHETER, MODEL SPK012008-09-30

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