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
1100459279
Device Listing 1100459279
Listing Summary
#
Listing key
1100459279
Premarket submission
K984129
Device
COAGULATION CONTROL LEVEL 1 (NORMAL)
Applicant
Pacific Hemostasis
Product code
GIZ
Decision date
1998-12-01
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
7647
1181121
1181121
Fisher Diagnostics
1
Y
2026-01-01
8365 VALLEY PIKE MIDDLETOWN VA US 22645