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
1788415039
Device Listing 1788415039
Listing Summary
#
Listing key
1788415039
Premarket submission
K890443
Device
CASPAR SCALP CLIP, APPLIER
Applicant
Aesculap Instruments Corp.
Product code
HBO
Decision date
1989-06-15
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
38731
2916714
2916714
AESCULAP, INC.
1
Y
2026-01-01
3773 CORPORATE PKWY. CENTER VALLEY PA US 18034
38732
3003587896
3003587896
AESCULAP, INC.
1
N
2026-01-01
615 LAMBERT POINTE DR. HAZELWOOD MO US 63042