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
1911593394
Device Listing 1911593394
Listing Summary
#
Listing key
1911593394
Premarket submission
K955047
Device
WESTMED CIRCULARIE PEP DEVICES
Applicant
Westmed Intl.
Product code
BYE
Decision date
1996-03-27
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
46270
2028807
1000374126
WESTMED, INC.
1
N
2026-01-01
5580 S NOGALES HWY TUCSON AZ US 85706