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
1646100674
Device Listing 1646100674
Listing Summary
#
Listing key
1646100674
Premarket submission
K170183
Device
Cetus system, Cetus probe
Applicant
A.R.C Laser GmbH
Product code
HQE
Decision date
2017-09-27
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
25512
3006617841
3006617841
A.R.C. LASER GMBH
1
N
2026-01-01
BESSEMERSTRASSE 14 NUREMBERG BAVARIA DE 90411