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
2073238022
Device Listing 2073238022
Listing Summary
#
Listing key
2073238022
Premarket submission
K111254
Device
RELIEVA SOLO ELITE SINUS BALLOON CATHETER
Applicant
Acclarent, Inc.
Product code
LRC
Decision date
2011-08-22
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
189329
3005172759
3005172759
ACCLARENT, INC.
1
Y
2026-01-01
7585 Irvine Center Dr Irvine CA US 92618