510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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OXWNot classified

Stimulator, Electrical, Transcutaneous, For Diabetic Retinopathy

Unknown
FDA source (opens on fda.gov)

OXW is the FDA product code for Stimulator, Electrical, Transcutaneous, For Diabetic Retinopathy. FDA's definition for this code reads: "Electrical stimulation unit with leads and cutaneous electrodes used to apply an electrical current through the electrodes to the patient's eyelid to create a microcurrent loop that flows through the retina". As of , FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code
OXW
Device name
Stimulator, Electrical, Transcutaneous, For Diabetic Retinopathy
FDA definition
Electrical stimulation unit with leads and cutaneous electrodes used to apply an electrical current through the electrodes to the patient's eyelid to create a microcurrent loop that flows through the retina.
Device class
Not classified
Review panel
Unknown
Submission type
Contact ODE
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
0

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code OXW.