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
1981762318
Device Listing 1981762318
Listing Summary
#
Listing key
1981762318
Premarket submission
K122791
Device
LYOPLANT ONLAY
Applicant
Aesculap, Inc.
Product code
GXQ
Decision date
2013-06-04
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
9103
9610612
3002806315
AESCULAP AG
1
N
2027-01-01
AM AESCULAP PLATZ TUTTLINGEN, DONAU Baden-Wurttemberg DE D-78532