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
1099585898
Device Listing 1099585898
Listing Summary
#
Listing key
1099585898
Premarket submission
K922176
Device
INTELIJET SUCTION SUPPLY
Applicant
Smith & Nephew Dyonics, Inc.
Product code
BTA
Decision date
1992-11-18
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