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
1874009622
Device Listing 1874009622
Listing Summary
#
Listing key
1874009622
Premarket submission
K923768
Device
PULSE CRP TEST
Applicant
Pulse Scientific, Inc.
Product code
DCK
Decision date
1992-12-01
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
302226
3017505309
3017505309
KSL Biomedical, Inc.
1
N
2026-01-01
55 Amherst Villa Road Buffalo NY US 14225