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
1137238142
Device Listing 1137238142
Listing Summary
#
Listing key
1137238142
Premarket submission
K924516
Device
OP3/VP4
Applicant
Huntleigh Technology, Inc.
Product code
HGL
Decision date
1993-06-28
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
39874
1000589001
1000589001
Darren DeMerritt
1
N
2026-01-01
2000 Center Drive Suite D403 Hoffman Estates IL US 60192