FDA Adverse Event Injury Summary report: N

ASPEN SURGICAL SYSTEMS

MDR report key: 175586 · Received July 2, 1998

Report

Report Number
1720159-1998-00042
Event Type
Injury
Date Received
July 2, 1998
Date of Event
May 29, 1998
Manufacturer
ASPEN LABORATORIES, INC
Product Code
GEI
Removal / Correction Number
NA
Report Source
Manufacturer report

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ASPEN SURGICAL SYSTEMS ELECTROSURGICAL PENCIL GEI ASPEN LABORATORIES, INC HAND-TROL UNK

Patients

Seq Age Sex Outcome Treatment
1