MAUDE report
MAUDE report 10203: INTERFERENTIAL STIMULATION
Other · received Aug 17, 1993 · METTLER ELECTRONICS CORP.
Key facts
| MDR report key | 10203 |
|---|---|
| Report number | 10203 |
| Event type | Other |
| Brand name | INTERFERENTIAL STIMULATION |
| Model number | SYS* STIM 220 |
| Manufacturer | METTLER ELECTRONICS CORP. |
| Product code | LPY |
| Date received by FDA | Aug 17, 1993 |
| Report date | Apr 29, 1993 |
| Report source | Maude |
At a glance
- None Device problems coded
- 1–9 MAUDE reports for this product code
- 1–9 MAUDE reports for this brand
- None Death reports for this brand
- None Injury reports for this brand
- Yes Adverse event flagged
- No Product problem flagged
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About MAUDE medical device reports
MAUDE holds medical device reports (MDRs) of suspected device-associated deaths, serious injuries and malfunctions submitted to the FDA by manufacturers, importers, user facilities and the public. A report alone does not establish that a device caused an event.
Source: U.S. Food and Drug Administration (FDA), MAUDE (Manufacturer and User Facility Device Experience) database · Source date: