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
1573431071
Device Listing 1573431071
Listing Summary
#
Listing key
1573431071
Premarket submission
K970187
Device
RUNYON LARGE VOLUME PARACENTESIS KIT
Applicant
Gi Supply
Product code
LRO
Decision date
1997-02-14
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
27944
2523676
2523676
B. BRAUN US DEVICE MANUFACTURING LLC
1
N
2026-01-01
901 Marcon Blvd ALLENTOWN PA US 18109