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
1809810324
Device Listing 1809810324
Listing Summary
#
Listing key
1809810324
Premarket submission
K925361
Device
BIOPSY FORCEPS, ELECTRIC
Applicant
United States Endoscopy Group, Inc.
Product code
KGE
Decision date
1993-03-29
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
202153
1528319
1000122656
UNITED STATES ENDOSCOPY GROUP, INC.
1
N
2020-04-25
5976 Heisley Rd Mentor OH US 44060