FDA Device Establishments · JSON-LD · Markdown

AMREX-ZETRON, INC.

FEI 2011115 · Manufacture Medical Device · Status: Active

FEI Number2011115
Owner / OperatorAMREX-ZETRON, INC. (#2011115)
Address7034 Jackson St, Paramount, CA, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)IMI
Regulation § (21 CFR)890.5300
Proprietary namesAMREX SYNCHROSONIC U/20 PORTABLE ULTRASOUND; AMREX SYNCHROSONIC U/50; SYNCHROSONIC; AMREX SYNCHROSONIC 210C; AMREX SYNCHROSONIC 210; AMREX SYNCHROSONIC US/50 COMBINATION ULTRASOUND / LOW VOLT AC STIMULATOR; AMREX SYCHROSONIC US/752 COMBINATION ULTRASOUND/HIGH VOLT PULSED DC STIMULATOR; AMREX SYNCHROSONIC U/20; AMREX SYNCHROSONIC 210 RX; AMREX SYNCHROSONIC U200

External sources

Source: openFDA. Public-domain (CC0).