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
1595007207
Device Listing 1595007207
Listing Summary
#
Listing key
1595007207
Premarket submission
K870562
Device
DAIG PACEMAKER LEAD ADAPTOR
Applicant
Daig Corp.
Product code
DTD
Decision date
1987-03-03
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
105721
2183787
2183787
Greatbatch Medical
1
Y
2026-01-01
2300 Berkshire Lane North Minneapolis MN US 55441