FDA.reportPublic FDA data

Matthew Walenciak

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30057784703005778470Matthew Walenciak1N2020-04-257900 Triad Center Drive Suite 400 Greensboro NC US 27409
30079669293007966929Matthew Walenciak1N2020-04-257900 Triad Center Drive Suite 400 Greensboro NC US 27409

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
98991958211118K896734FEEDING TUBEFPD1990-12-21
98991062049851K896729NELATON-, FEMALE - OR TIEMANN CATHETERKOD1990-11-05
98991736914803K873286DISPOSABLE, MANUAL PULMONARY RESUSCITATORBTM1987-10-26
1094131519889704K842395SUR-FIT NIGHT DRAINAGE CONTAINER SETKNX1984-08-08
98991546689553K181206GentleCath Glide Intermittent Urinary CatheterGBM2018-08-16
98991751779980K172924GentleCath Intermittent Urinary CatheterKOD2017-11-21
98991612478933K161344GentleCath Glide Intermittent CatheterKOD2016-09-20
1094131050013298
1094131084359034
1094131128793855
98991162239373
98991411068312
98991433922938
98991441446639
1094131507721122
1094131515507480
1094131542020585
1094131580661017
98991718859054
98991769812937
98991774570879
98991785935471
1094131882073882
98991890733948
98991953176799
1094132001073682
1094132058761811

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
KOD32017-11-21
GBM12018-08-16
FPD11990-12-21
BTM11987-10-26
KNX11984-08-08