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
1717376599
Device Listing 1717376599
Listing Summary
#
Listing key
1717376599
Premarket submission
K933732
Device
BEECH PROLOK
Applicant
Beech Medical, Inc.
Product code
FPA
Decision date
1993-12-29
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
82191
1221765
1221765
MULTI-MED, INC.
1
N
2026-01-01
26 Victoria Ct Keene NH US 03431