FDA Adverse Event
Malfunction
Summary report: N
1036844-2008-00137
MDR report key: 1231875
·
Received August 1, 2008
Report
- Report Number
- 1036844-2008-00137
- Event Type
- Malfunction
- Date Received
- August 1, 2008
- Product Code
- DQO
- PMA / PMN Number
- K862056
- Removal / Correction Number
- NA
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
FOLLOW-UP REPORT WILL BE FILED IF ADDITIONAL INFO BECOMES AVAILABLE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | DQO |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |