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
1334320198
Device Listing 1334320198
Listing Summary
#
Listing key
1334320198
Premarket submission
K181122
Device
CARDIOSAVE Intra-Aortic Balloon Pump
Applicant
Datascope Corp.
Product code
DSP
Decision date
2018-05-31
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
235808
3007965489
3007965489
Datascope Corp
1
N
2020-04-25
45 Barbour Pond Drive Wayne NJ US 07470