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
1663560620
Device Listing 1663560620
Listing Summary
#
Listing key
1663560620
Premarket submission
K230428
Device
Ambu® aScope™ 5 Broncho 2.7/1.2, Ambu® aScope™ 5 Broncho 4.2/2.2, Ambu® aBox™ 2
Applicant
Ambu A/S
Product code
EOQ
Decision date
2023-08-10
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
80359
9610691
3002806359
Ambu A/S
1
N
2026-01-01
Baltorpbakken 13 Ballerup Hovedstaden DK DK-2750
39870
3004040397
3004040397
Sanjay Parikh
1
N
2026-01-01
6721 Columbia Gateway Drive, Suite 200 Columbia MD US 21046