FDA Adverse Event
Malfunction
Summary report: N
9611369-2008-00146
MDR report key: 1011753
·
Received February 20, 2008
Report
- Report Number
- 9611369-2008-00146
- Event Type
- Malfunction
- Date Received
- February 20, 2008
- Product Code
- KDI
- PMA / PMN Number
- K010667
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
NO FURTHER INFO IS EXPECTED FOR THIS SPECIFIC EVENT AND THE CASE IS CONSIDERED CLOSED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | KDI |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |