FDA Adverse Event
Summary report: N
MICROVAS
MDR report key: 597105
·
Received April 19, 2005
Report
- Report Number
- MW4003923
- Date Received
- April 19, 2005
- Report Date
- March 15, 2005
- Manufacturer
- MICROVAS
- Product Code
- GZC
- Report Source
- Voluntary report
- Reporter Location
- OK, US
- Reporter Occupation
- PATIENT
Narratives
Description of Event or Problem · 1
WAS INTERESTED IN GETTING TREATMENTS FROM THE FIRM'S DEVICE BECAUSE HAS NEUROPATHY. FIRM SENT MATERIAL CLAIMING TO CURE 84 DISEASES AND THAT 4-5 PROBLEMS CAN BE TREATED AT ONCE. THOUGHT THESE CLAIMS WERE MISLEADING.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | MICROVAS | ELECTRICAL MUSCLE STIMULATOR | GZC | MICROVAS | * | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * |