FDA.reportPublic FDA data

GYRUS ACMI L.P.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30059754943011050570GYRUS ACMI L.P.1Y2020-04-259600 Louisiana Avenue North Brooklyn Park MN US 55445

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1431341671352102K980366AARON 1200 HIGH FREQUENCY ELECTROSURGICL GENERATOR A1200, A1200/240GEI1998-02-27
1431341741129826K945262OPTUS CYSTOSCOPES AND PEDIATRIC CYSTOSCOPESFAJ1995-05-26
1431341300088907K941952SURGITEK INFUSERFAD1994-05-24
1431341316799100K022543ARTHROCARE BIPOLAR ELECTROSURGERY SYSTEMFAS2002-08-30
1431341154497263
1431341589379174

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
FAS12002-08-30
GEI11998-02-27
FAJ11995-05-26
FAD11994-05-24