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
1176495745
Device Listing 1176495745
Listing Summary
#
Listing key
1176495745
Premarket submission
K152547
Device
DNAP Electrode
Applicant
Ad-Tech Medical Instrument Corporation
Product code
GZL
Decision date
2016-03-04
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
6102
2183456
2183456
AD-TECH MEDICAL INSTRUMENT CORP.
1
N
2026-01-01
400 West Oakview Parkway Oak Creek WI US 53154