FDA Adverse Event Other Summary report: N

2182207-1997-00023

MDR report key: 82756 · Received April 8, 1997

Report

Report Number
2182207-1997-00023
Event Type
Other
Date Received
April 8, 1997
Date of Event
November 12, 1996
Manufacturer
MEDTRONIC INC.
Product Code
GZB
Report Source
Manufacturer report

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 GZB MEDTRONIC INC.

Patients

Seq Age Sex Outcome Treatment
1 *