FDA Adverse Event Injury Summary report: N

2182596-1997-00320

MDR report key: 87884 · Received April 30, 1997

Report

Report Number
2182596-1997-00320
Event Type
Injury
Date Received
April 30, 1997
Date of Event
January 1, 1983
Product Code
FTR
Report Source
Manufacturer report
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

ALLEGATIONS OF SCELRDERMA.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 Implant FTR

Patients

Seq Age Sex Outcome Treatment
1 *