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
1926639843
Device Listing 1926639843
Listing Summary
#
Listing key
1926639843
Premarket submission
K173937
Device
SpiroSphere
Applicant
Eresearchtechnology GmbH
Product code
BTY
Decision date
2019-02-15
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
124820
3008505660
3008505660
Todd Kisner
1
N
2026-01-01
1818 Market Street, Suite 2600 Philadelphia PA US 19103