FDA.reportPublic FDA data

PROTEK MEDICAL PRODUCTS, INC.

Matched from indexed company URL: PROTEK, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
19340293001701594PROTEK MEDICAL PRODUCTS, INC.1N2020-04-254125 WESTCOR COURT CORALVILLE IA US 52241

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
532301699601187K973958GENERAL PURPOSE ATL NEEDLE GUIDE KITITX1998-01-22
532301424466367K973622TRANSDUCER POSITIONERITX1997-11-26
532302007256412K973362NEEDLE GUIDE/GRIDITX1997-10-01
532301512458461K971722TRANS VAGINAL NEEDLE GUIDEITX1997-07-10
532301641302779K971115GE MEDICAL-NEEDLE GUIDE FOR SV, TR ANDATF, ACUSON-NEEDLE GUIDEITX1997-06-13
532301151582274K970893ULTRASOUND TRANSDUCER DRAPEFYA1997-10-20
532301236837137K970891DRAPE, SURGICAL-LATEXKKX1997-08-22
532301358925253K970889ULTRASOUND TRANSDUCER DRAPEKKX1997-10-20
532301221565382K970885ULTRASOUND SYSTEMS DRAPEMMP1997-09-22

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
ITX51998-01-22
KKX21997-10-20
FYA11997-10-20
MMP11997-09-22

NDC#

PMN#

GUDID#

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