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
1755094832
Device Listing 1755094832
Listing Summary
#
Listing key
1755094832
Premarket submission
K202391
Device
DIR 800
Applicant
Aesculap, Inc.
Product code
IZI
Decision date
2021-01-21
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
9103
9610612
3002806315
Kamaal Anas
1
N
2026-01-01
3773 Corporate Parkway Center Valley PA US 18034