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
1935525197
Device Listing 1935525197
Listing Summary
#
Listing key
1935525197
Premarket submission
K143700
Device
CPAP Cannulaide
Applicant
Salter Labs
Product code
BZD
Decision date
2015-08-05
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
325185
3030446844
3030446844
PLATINUM FOCUS GROUP LTD.
1
N
2026-01-01
Unit 5, 1000 North Circular Road London London, City of GB NW2 7JP