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
1062653040
Device Listing 1062653040
Listing Summary
#
Listing key
1062653040
Premarket submission
K973537
Device
PATHWAY ELECTROMYOGRAPH
Applicant
The Prometheus Group
Product code
HCC
Decision date
1997-12-17
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
16001
1224842
1000513601
THE PROMETHEUS GROUP
1
N
2026-01-01
1 WASHINGTON ST., SUITE 3171 DOVER NH US 03820