FDA.reportPublic FDA data

ANALOG DEVICES

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30001308293000130829ANALOG DEVICES1N2026-01-01One Analog Way Wilmington MA US 01887

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
3255381064756393K243216Sensinel Cardiopulmonary Management (CPM) System (ADCP1100)MWI2024-12-10
3255381233211103K231086CPM SystemMWI2023-12-22

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
MWI22024-12-10

PMN#

GUDID#