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
2047989210
Device Listing 2047989210
Listing Summary
#
Listing key
2047989210
Premarket submission
K053160
Device
MICRUS MODIFIED MICROCOIL 18-SYSTEM, CERECYTE, MODEL CSP & CHE
Applicant
Micrus Endovascular Corporation
Product code
HCG
Decision date
2005-12-07
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
210440
3013875781
3013875781
Codman & Shurtleff, Inc.
1
N
2020-04-25
47709 Fremont Blvd. Fremont CA US 94538