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
1587504351
Device Listing 1587504351
Listing Summary
#
Listing key
1587504351
Premarket submission
K100078
Device
MODIFIED STRAIGHT FIRE LASER FIBER
Applicant
Boston Scientific Corp
Product code
GEX
Decision date
2010-02-12
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
161726
3010405359
3010405359
COHERENT INC.
1
N
2020-04-25
32 Hampshire Rd Salem NH US 03079