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
1770900112
Device Listing 1770900112
Listing Summary
#
Listing key
1770900112
Premarket submission
K160328
Device
DIVA ZSP2105CMI with QUBYX PerfectLum bundle
Applicant
The Linden Group Corp
Product code
PGY
Decision date
2016-02-25
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
106839
3007817002
3007817002
DIVA LABORATORIES, LTD.
1
N
2020-04-25
9F. NO.351, SEC.2 ZHONGSHAN ROAD ZHONGHE DIST. NEW TAIPEI CITY, TAIPEI-DISTRICT, 235 Ta TW 235