FDA.reportPublic FDA data

Jeffrey Duncan

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
96111783002809579Jeffrey Duncan1N2020-04-256000 Nathan Ln N Minneapolis MN US 55442
96176463005580752Jeffrey Duncan1N2020-04-256000 Nathan Ln N Minneapolis MN US 55442

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
97042018058014K993619CSECURE COMBINED SPINAL/EPIDURAL ANESTHESIA SYSTEM WITH LOCKBSP2000-04-28
97151979505141K960515PARAPACBTL1996-10-10
97041607326188K862167MINI-TRACH KITBTO1986-08-06
97151055034103K123957PNEUPAC PARAPAC PLUSBTL2013-09-16
97151554333464K071527PNEUPAC VR1 AIR MIXBTL2007-10-04
97151515915979K051322PNEUPAC VRI STANDARD, MODEL VRISTDNUS, PNEUPAC VRI RESPONDER, MODEL VRIRESNUSBTL2005-08-05
97151159656387K043495BABYPACBTL2005-04-22
97041836204130K041348PORTEX ULTRAPERC PERCUTANEOUS DILATION TRACHEOSTOMY KIT_WITH SERIAL DILATORS OR SINGLE STAGE DILATOR, BLUE LINE ULTRAJOH2004-07-13
97151049660912K030803PARAPAC 200D TRANSPORT, MODEL V200DBTL2003-09-29
97151658288069K020899PARAPAC 200 MEDIC, MODEL P200, & PARAPAC 200D MEDIC, MODEL P200DBTL2002-12-13

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
BTL72013-09-16
JOH12004-07-13
BSP12000-04-28
BTO11986-08-06