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
1965919102
Device Listing 1965919102
Listing Summary
#
Listing key
1965919102
Premarket submission
K982149
Device
SMITH & NEPHEW DYONICS MICROLAPAROSCOPE
Applicant
Smith & Nephew, Inc.
Product code
HET
Decision date
1998-09-10
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
149134
1643264
1643264
SMITH & NEPHEW INC.
1
Y
2026-01-01
ENDOSCOPY 76 S. MERIDIAN AVE. OKLAHOMA CITY OK US 73107