MAUDE report
MAUDE report 5200
Malfunction · received Apr 27, 1993 · PENTAX
Key facts
| MDR report key | 5200 |
|---|---|
| Report number | 5200 |
| Event type | Malfunction |
| Model number | OF B78 |
| Manufacturer | PENTAX |
| Date received by FDA | Apr 27, 1993 |
| Report date | Mar 23, 1993 |
| Report source | Maude |
At a glance
- None Device problems coded
- No Adverse event flagged
- Yes 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: