FDA Adverse Event Other Summary report: N

2915274-2017-00006

MDR report key: 6579824 · Received May 19, 2017

Report

Report Number
2915274-2017-00006
Event Type
Other
Date Received
May 19, 2017
Date of Event
February 10, 2017
Report Date
March 1, 2017
Manufacturer
BIO-RAD LABORATORIES INC., CLINICAL SYSTEMS DIVISI
PMA / PMN Number
K031043
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER
Health Professional
N

Patients

Seq Age Sex Outcome Treatment
1 Unknown Other