FDA Adverse Event
Injury
Summary report: N
2242445-2008-00037
MDR report key: 1226043
·
Received October 31, 2008
Report
- Report Number
- 2242445-2008-00037
- Event Type
- Injury
- Date Received
- October 31, 2008
- Product Code
- DYG
- PMA / PMN Number
- K833572
- Removal / Correction Number
- NA
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
SAMPLE WILL NOT BE RETURNED FOR EVAL.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | DYG |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |