NEUROVIRTUAL USA, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30061253623006125362NEUROVIRTUAL USA, INC.1Y2026-01-013303 W Commercial Blvd Suite 100 Fort Lauderdale FL US 33309

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
672031930255771K201495Maxxi Flow SensorMNR2020-12-14
672031482336953K192488CO2 Sidestream ModuleCCK2020-05-22
672031344259513K191492Maxxi Position SensorGWQ2020-04-24
672031016891478K191095Maxxi Snore SensorMNR2020-01-16
672031008841384K171304Maxxi Rip SensorMNR2019-06-24
672031232302534K163547MaxxiGold Electrode 48, MaxxiGold Electrode 60, MaxxiGold Electrode 96GXY2017-04-11
672031693998689K131335BWMINI EEG, BWMINIHST, BWMINI PSGGWQ2015-02-03
672031240543280K112107BWIII EEG, BWIII EEG PLUS, BWIII PSG, BWIII PSG PLUSGWQ2011-10-28
672031470121886K083010SHENZHEN MED-LINKET ADULT FINGER CLIP SPO2 SENSOR, SHENZHEN MED-LINKET ADULT SILICONE SOFT TIP SPO2 SENSORDQA2009-06-10
672031774563224

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
MNR32020-12-14
GWQ32020-04-24
CCK12020-05-22
GXY12017-04-11
DQA12009-06-10

PMN#

GUDID#

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