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
1751079375
Device Listing 1751079375
Listing Summary
#
Listing key
1751079375
Premarket submission
K002788
Device
KSEA NEURO-FIBERSCOPE
Applicant
KARL STORZ Endoscopy-America, Inc.
Product code
GWG
Decision date
2000-10-23
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
12472
1221826
1221826
KARL STORZ ENDOVISION, INC.
1
N
2020-04-25
91 Carpenter Hill Rd CHARLTON MA US 01507