Matthew Walenciak

FDA Registration(s)

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 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 codeRegistration listing recordsLatest decision
KOD32017-11-21
GBM12018-08-16
FPD11990-12-21
BTM11987-10-26
KNX11984-08-08