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
1073603795
Device Listing 1073603795
Listing Summary
#
Listing key
1073603795
Premarket submission
K183285
Device
cmTriage
Applicant
Curemetrix, Inc.
Product code
QFM
Decision date
2019-03-08
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
275557
3017173128
3017173128
CUREMETRIX, INC.
1
N
2026-01-01
402 West Broadway Suite 400 San Diego CA US 92101