JAGISON MICROCURRENT PULSE STIMULATION
Received Aug 10, 2006
Report MW4004244 · MDR key 773224
Product problems
- Nonstandard Device
Patient
*
- Therapeutic Response, Decreased
Narrative
Description of Event or Problem
THE PRODUCT IS ADVERTISED AS BEING A PAIN RELIEVER AND IT DID NOT RELIEVE HIS PAIN. HE BELIEVES THAT THE PRODUCT IS NOT REGISTERED WITH THE FDA AND IS BEING SOLD AS AN UNAPPROVED MEDICAL DEVICE. NO INJURY OR ILLNESS REPORTED.