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
1946585197
Device Listing 1946585197
Listing Summary
#
Listing key
1946585197
Premarket submission
K010372
Device
LIGHTLAS 532 PHOTOCOAGULATOR
Applicant
Lightmed Corp.
Product code
HQF
Decision date
2001-08-22
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
110973
3008156177
3003559308
LIGHTMED CORP.
1
N
2026-01-01
No.1-1, Lane 1, Sec. 3, Pao An St., Shulin District New Taipei City TW 23861