FDA.reportPublic FDA data

ATHELAS

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30134452203013445220ATHELAS1N2026-01-011300 Terra Bella Ave STE 200 Mountain View CA US 94043
30165926723016592672ATHELAS1N2020-04-251270 Lawrence Station Rd Sunnyvale CA US 94089

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2006601861771145K243348Athelas HomeGKZ2026-02-06
2006602003427155K202891Blood Pressure MonitorDXN2021-03-09
2006601306324785K200828Athelas HomeGKZ2022-03-22
2006602031315888K181288Athelas OneGKZ2018-11-05
2384952031315888K181288Athelas OneGKZ2018-11-05

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
GKZ52026-02-06
DXN12021-03-09

PMN#

GUDID#