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
1471479519
Device Listing 1471479519
Listing Summary
#
Listing key
1471479519
Premarket submission
K190525
Device
RELIEVA ULTIRRA Sinus Balloon Catheter
Applicant
Acclarent, Inc.
Product code
LRC
Decision date
2019-05-03
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