FDA.reportPublic FDA data

HANS RUDOLPH, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
19225531922553HANS RUDOLPH, INC.1N2026-01-018325 COLE PKWY Shawnee KS US 66227

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
335701567028891K0308227600 SERIES MULTI-PATIENT MULTI-USE ORO-NASAL CPAP/NPPV MASKSBZD2003-06-03
335701133072402K030515HANS RUDOLPH 7500 SERIES REUSABLE ORO-NASAL NIV MASKSCBK2003-05-02
335701028450835
335701118044180
335701250817056
335701419950203
335701456400940
335701457215443
335701484073500
335701499935173
335701633613913
335702033392577
335701428473742
335701659492069
335701796208760

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
BZD12003-06-03
CBK12003-05-02

PMN#

GUDID#

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