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
1962545169
Device Listing 1962545169
Listing Summary
#
Listing key
1962545169
Premarket submission
K113255
Device
PUREGRAFT 850/PURE SYSTEM
Applicant
Cytori Therapeutics, Inc.
Product code
MUU
Decision date
2012-03-07
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
177315
3011277972
3011277972
PUREGRAFT LLC
1
Y
2020-04-25
420 Stevens Ave Ste 220 Solana Beach CA US 92075