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
1194186863
Device Listing 1194186863
Listing Summary
#
Listing key
1194186863
Premarket submission
K992130
Device
PACIFIC HEMOSTASIS THROMBOSCREEN 400C
Applicant
Pacific Hemostasis
Product code
KQG
Decision date
1999-09-03
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