FDA Adverse Event Other Summary report: N

9610617-2000-00027

MDR report key: 302638 · Received October 27, 2000

Report

Report Number
9610617-2000-00027
Event Type
Other
Date Received
October 27, 2000
Date of Event
September 27, 2000
Product Code
FFK
Report Source
Manufacturer report

Devices

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

Patients

Seq Age Sex Outcome Treatment
1