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
1038344988
Device Listing 1038344988
Listing Summary
#
Listing key
1038344988
Premarket submission
K251037
Device
Rectal Applicator
Applicant
Nucletron B.V.
Product code
JAQ
Decision date
2025-12-19
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
10635
9611894
3002807741
NUCLETRON B.V.
1
N
2026-01-01
3900 AX VEENENDAAL, P.O. BOX 930 Waardgelder 1 VEENENDAAL Utrecht NL 3905 TH