FDA Adverse Event
Other
Summary report: N
2024841-2001-00001
MDR report key: 318331
·
Received March 2, 2001
Report
- Report Number
- 2024841-2001-00001
- Event Type
- Other
- Date Received
- March 2, 2001
- Date of Event
- January 30, 2001
- Product Code
- BTO
- Report Source
- Manufacturer report
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 9135 | BTO |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |