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
1705683363
Device Listing 1705683363
Listing Summary
#
Listing key
1705683363
Premarket submission
K082556
Device
CLEARCORRECT
Applicant
Clearcorrect, Inc.
Product code
NXC
Decision date
2009-02-06
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
91448
3007130440
3007130440
CLEARCORRECT LLC
1
N
2020-04-25
21 Cypress Blvd Ste 1010 Round Rock TX US 78665