FDA.reportPublic FDA data

GTIMD LLC

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30094323253009432325GTIMD LLC1N2020-04-256 Columbia Dr Unit B Amherst NH US 03031

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1976241469183208K981936ABD VARISOFT STEERABLE GUIDE WIRE AND ABD VARISOFT GUIDE WIRE EXTENSIONDQX2000-02-16
1976241387708357K160664Aqueduct 100 Cervical DilatorPON2016-08-01

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
PON12016-08-01
DQX12000-02-16

PMN#