FDA.reportPublic FDA data

Device Listing 1078080828

Listing Summary#

Listing key
1078080828
Premarket submission
K132186
Device
OPTOMED SMARTSCOPE M5 / OPTOMED SMARTSCOPE EY4 / OPTOMED SMARTSCOPE ES2
Applicant
Optomed OY
Product code
HKI
Decision date
2013-12-18