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
1807233330
Device Listing 1807233330
Listing Summary
#
Listing key
1807233330
Premarket submission
K222297
Device
CentriMag Pre-connected Pack
Applicant
Abbott
Product code
DTZ
Decision date
2022-12-01
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
216414
1218444
1218444
THORATEC CORP
1
N
2026-01-01
23 4th Ave BURLINGTON MA US 01803
216415
2916596
2916596
THORATEC CORP.
1
N
2026-01-01
6035 Stoneridge Dr PLEASANTON CA US 94588