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
1933851935
Device Listing 1933851935
Listing Summary
#
Listing key
1933851935
Premarket submission
P130019
Device
MAESTRO RECHARGEABLE SYSTEM
Applicant
ReShape Lifesciences, Inc.
Product code
PIM
Decision date
2015-01-14
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
140204
3005025697
3005025697
ReShape Lifesciences, LLC.
1
N
2020-04-25
2800 Patton Rd Suite B Saint Paul MN US 55113