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
1723294675
Device Listing 1723294675
Listing Summary
#
Listing key
1723294675
Premarket submission
K020482
Device
KERATOME BLADE 200200 & 600600
Applicant
Micro Specialties, Inc.
Product code
HNO
Decision date
2002-12-16
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
203342
1226074
3002616700
Microspecialties LLC
1
N
2026-01-01
430 Smith St Middletown CT US 06457