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
1105385188
Device Listing 1105385188
Listing Summary
#
Listing key
1105385188
Premarket submission
K241764
Device
Mould Probe MR Safe
Applicant
Varian Medical Systems, Inc.
Product code
JAQ
Decision date
2025-01-10
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
286590
3016602874
3016602874
Varian Medical Systems Haan GmbH
1
N
2026-01-01
Rheinische Strasse 2 Haan North Rhine-Westphalia DE 42781