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
1774257106
Device Listing 1774257106
Listing Summary
#
Listing key
1774257106
Premarket submission
K970211
Device
MICROLIFE AUTOMATIC BLOOD PRESSURE MONITOR
Applicant
Micro Weiss Electronics
Product code
DPW
Decision date
1998-04-30
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
130077
3006537699
3006537699
KELLY GEYER-MEDINA
1
N
2026-01-01
312 Raleigh St Ste 9 Wilmington NC US 28412