FDA Adverse Event Other Summary report: N

IPC 5000

MDR report key: 559252 · Received November 25, 2003

Report

Report Number
559252
Event Type
Other
Date Received
November 25, 2003
Date of Event
November 22, 2003
Report Date
November 25, 2003
Manufacturer
CLINICAL INNOVATIONS, INC.
Product Code
HDT
Report Source
User Facility report
Reporter Location
IN, US

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 IPC 5000 INTRAUTERINE PRESSURE SYSTEM HDT CLINICAL INNOVATIONS, INC. * 030664

Patients

Seq Age Sex Outcome Treatment
1 * NO OTHER THERAPIES