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
1299266761
Device Listing 1299266761
Listing Summary
#
Listing key
1299266761
Premarket submission
K994299
Device
ART-P3, MODEL P3-1-ART-A1
Applicant
Bonart Co., Ltd.
Product code
ELC
Decision date
2000-03-06
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
57015
9710363
3008981576
BONART CO. LTD.
1
N
2027-01-01
NO.80, WUXUN STREET ANLE DISTRICT KEELUNG TW 20446