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
1372636082
Device Listing 1372636082
Listing Summary
#
Listing key
1372636082
Premarket submission
K991321
Device
PACIFIC HEMOSTASIS THROMBOSCREEN 200
Applicant
Pacific Hemostasis
Product code
KQG
Decision date
1999-06-21
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