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
1551927002
Device Listing 1551927002
Listing Summary
#
Listing key
1551927002
Premarket submission
K092135
Device
MODIFICATION TO IVENT 101
Applicant
Versamed Medical Systems , Ltd.
Product code
CBK
Decision date
2009-11-23
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
26621
2112667
2112667
Datex-Ohmeda, Inc.
1
Y
2026-01-01
3030 Ohmeda Drive MADISON WI US 53718