FDA Adverse Event Other Summary report: N

*

MDR report key: 601201 · Received February 14, 2005

Report

Report Number
1924066-2005-00001
Event Type
Other
Date Received
February 14, 2005
Date of Event
October 31, 2004
Manufacturer
ALLIED HEALTHCARE PRODUCTS, INC.
Product Code
CAN
Report Source
Manufacturer report
Reporter Occupation
INVALID DATA

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 * * CAN ALLIED HEALTHCARE PRODUCTS, INC. * *

Patients

Seq Age Sex Outcome Treatment
1 *