FDA Adverse Event Summary report: N

UNK

MDR report key: 807292 · Received January 10, 2007

Report

Report Number
807292
Date Received
January 10, 2007
Date of Event
September 22, 2006
Report Date
January 10, 2007
Manufacturer
UNK
Product Code
JXK
Report Source
User Facility report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

BRAIN STIMULATOR.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 UNK UNK JXK UNK UNK UNK

Patients

Seq Age Sex Outcome Treatment
1 67 YR