FDA.reportPublic FDA data

CME AMERICA, LLC

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30069677103006967710CME AMERICA, LLC1N2020-04-2514998 W 6TH AVE STE 830 Golden CO US 80401

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
B101100100POBSC0T34 Syringe Pump System - Pump, Operator's Manual303-936-4945xx@xx.xx
B101100100PSA0T34 Syringe Pump System - Pump, Operator's Manual303-936-4945xx@xx.xx

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
898341290086963K080954T34L SYRINGE DRIVERFRN2008-05-16
898341733280905K042696BODYGUARD INFUSION PUMP SYSTEMFRN2005-03-11

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
FRN22008-05-16

GUDID#

193 records. Showing 1-40. Next