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
1631788876
Device Listing 1631788876
Listing Summary
#
Listing key
1631788876
Premarket submission
K982462
Device
FIBER OPTIC ENDOILLUMINATION PROBE
Applicant
Microvision, Inc.
Product code
FFS
Decision date
1998-09-14
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
21269
3002991496
3002991496
Paul Swift
1
N
2026-01-01
5300 Central Pkwy Dublin CA US 94568