FDA Adverse Event
Other
Summary report: N
INTELECT XT
MDR report key: 1012372
·
Received March 7, 2008
Report
- Report Number
- 1022819-2008-00082
- Event Type
- Other
- Date Received
- March 7, 2008
- Date of Event
- February 26, 2008
- Report Date
- March 6, 2008
- Manufacturer
- CHATTANOOGA GROUP
- Product Code
- IPF
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- OR, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
AWAITING RETURN AND EVAL OF THE DEVICE.
Description of Event or Problem · 1
PT REPORTED INCREASED SHOCKING SENSATION DURING TREATMENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | INTELECT XT | POWER MUSCLE STIMULATOR | IPF | CHATTANOOGA GROUP | 2760 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |