FDA Adverse Event Malfunction Summary report: N

4234107-PERQCATH 4FR D/L W/GW FU

MDR report key: 284904 · Received June 27, 2000

Report

Report Number
1720496-2000-00462
Event Type
Malfunction
Date Received
June 27, 2000
Date of Event
April 24, 2000
Report Date
May 25, 2000
Product Code
DQO
Report Source
Manufacturer report

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 4234107-PERQCATH 4FR D/L W/GW FU LONG TERM INTRAVASCULAR DQO 4234107 36CK0094

Patients

Seq Age Sex Outcome Treatment
1