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
1695810434
Device Listing 1695810434
Listing Summary
#
Listing key
1695810434
Premarket submission
K821523
Device
OMNI TENS
Applicant
Omni Intl., Inc.
Product code
GZJ
Decision date
1982-06-16
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
33556
1911273
1000119345
ACCELERATED CARE PLUS CORP.
1
Y
2026-01-01
1170 Trademark Dr Ste 104 RENO NV US 89521