FDA Adverse Event Injury Summary report: N

2183541-1997-00011

MDR report key: 76078 · Received March 11, 1997

Report

Report Number
2183541-1997-00011
Event Type
Injury
Date Received
March 11, 1997
Date of Event
January 30, 1997
Product Code
MAF
Report Source
Manufacturer report

Devices

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

Patients

Seq Age Sex Outcome Treatment
1