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
1994680501
Device Listing 1994680501
Listing Summary
#
Listing key
1994680501
Premarket submission
K853608
Device
NEUROMETER
Applicant
Neurotron, Inc.
Product code
LLN
Decision date
1986-06-12
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
97600
1121806
1121806
Neurotron Inc
1
N
2026-01-01
12635 East Montview Blvd Suite 127 Aurora CO US 80045