Amrex-Zetron, Inc.
Paramount, CA, US
AMREX-ZETRON, INC. appears in FDA device records in Paramount, CA. FDA records list one 510(k) clearance, no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 1 510(k) clearance for Amrex-Zetron, Inc. in 1984.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1984 | 1 |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 2011115 | 2011115 | AMREX-ZETRON, INC. | 7034 Jackson St, Paramount, CA 90723 US | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- KTBDevice, Iontophoresis, Specific Uses
- IMJDiathermy, Shortwave, For Use In Applying Therapeutic Deep Heat
- IRPMassager, Powered Inflatable Tube
- GYBMedia, Electroconductive
- IPFStimulator, Muscle, Powered
- BXMStimulator, Nerve, Ac-Powered
- GZJStimulator, Nerve, Transcutaneous, For Pain Relief
- GZIStimulator, Neuromuscular, External Functional
- IMGStimulator, Ultrasound And Muscle, For Use In Applying Therapeutic Deep Heat
- IMIUltrasonic Diathermy For Use In Applying Therapeutic Deep Heat
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain