FDA.reportPublic FDA data

PATHWAY MEDTECH, LLC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30128330533012833053PATHWAY MEDTECH, LLC.1N2026-01-018779 Cottonwood Ave Ste 105 Santee CA US 92071

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1965081139475400K181616PSM 3-Way Silicone Foley CatheterEZL2018-09-21
1965081968468154K171880IRRAflow CNS SystemJXG2018-07-13
1965081700745518K162233Kurin Blood Culture Collection SetJKA2016-12-23
1965081613924113K142087COVA MONITORING SYSTEMMWI2015-05-01
1965081122646267K121554Q-FLO CLOSED MALE LUER CONNECTORFPA2012-06-08
1965081008587913
1965081675524112
1965081870032681
1965081102132358
1965081110357644
1965081220625964
1965081225476043
1965081416112109
1965081527068009
1965081543551773
1965081601202149
1965081822162366
1965081845929396
1965081874079708

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
EZL12018-09-21
JXG12018-07-13
JKA12016-12-23
MWI12015-05-01
FPA12012-06-08

GUDID#