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
2066013517
Device Listing 2066013517
Listing Summary
#
Listing key
2066013517
Premarket submission
K093617
Device
VENTLAB 6000 SERIES HUMIDIFIER
Applicant
Ventlab Corp.
Product code
BTT
Decision date
2011-01-27
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
36767
3005998497
3005998497
SUNMED AP, LTD.
1
N
2026-01-01
6-9 ZHUFENG RD., QIANNAN INDUSTRIAL PARK QIANWU TOWN, DOUMEN DISTRICT ZHUHAI Guangdong CN 519170