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
1422486217
Device Listing 1422486217
Listing Summary
#
Listing key
1422486217
Premarket submission
K080537
Device
L-VARLOCK
Applicant
Kiscomedica S.A.
Product code
MAX
Decision date
2008-06-30
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
170807
3010866843
3010866843
ACUITY SURGICAL DEVICES, LLC
1
N
2026-01-01
8710 N Royal Lane Irving TX US 75063