Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1235259632
Device Listing 1235259632
Listing Summary
#
Listing key
1235259632
Premarket submission
K041607
Device
QUINTON Q-TE; RMS
Applicant
Quinton Cardiology, Inc.
Product code
MHX
Decision date
2004-07-16
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
225678
2183461
2183461
Welch Allyn, Inc.
1
N
2020-04-25
7865 NORTH 86TH ST. MILWAUKEE WI US 53224