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
2065840080
Device Listing 2065840080
Listing Summary
#
Listing key
2065840080
Premarket submission
K183322
Device
physIQ Heart Rhythm and Respiratory Module
Applicant
Physiq, Inc.
Product code
DPS
Decision date
2019-07-10
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
326511
3030597723
3030597723
PROLAIO INC.
1
N
2026-01-01
230 W Monroe St Ste 2560 Chicago IL US 60606