FDA.reportPublic FDA data

BUNNELL, INC.

Matched from indexed company URL: Bunnell, Inc.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
17192321719232BUNNELL, INC.1N2020-04-25436 LAWNDALE DR. S Salt Lake UT US 84115

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
328641088487267P850064MODEL 203 LIFE PULSE HIGH FREQUENCY VENTILATORLSZ1988-06-30

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
LSZ11988-06-30

PMA#

LifePulse High Frequency Ventilator

2022-03-31

BUNNELL, INC.436 Lawndale Dr.salt Lake City, UT 84115 PMA NumberP850064 Supplement NumberS047 Date Received03/07/2022 Decision Date03/31/2022 Product Code LSZ  Advisory Committee Anesthesiology Supplement Type30-day Notice Supplement Reason Process Change -...

PMN#

GUDID#