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
1254851779
Device Listing 1254851779
Listing Summary
#
Listing key
1254851779
Premarket submission
K203623
Device
StentBoost Mobile
Applicant
Philips India Limited
Product code
OWB
Decision date
2021-04-05
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
183476
3010685285
3010685285
Philips India Limited
1
N
2026-01-01
Plot no. B-79, MIDC, Phase-II, Chakan Taluka - khed, Village - Savardari Pune Mah?r?shtra IN 410 501
333014
3033525987
3033525987
Maria Heiling
1
N
2026-01-01
3721 Valley Centre Dr Ste 500 San Diego CA US 92130