inforMED
KJFClass I

System, Suspension, Cell Culture

Hematology · 21 CFR 864.2240

MDR events3All time
Recalls0All time
Registered firms23Currently listed
510(k) clearances4All time

Event type breakdown

Malfunction3

Product problems

Reported product problem codes, most common first

Adverse Event Without Identified Device or Use Problem2
Break1
Contamination1
Contamination /Decontamination Problem1

Trend for “Adverse Event Without Identified Device or Use Problem

No history to chart.

Recalls

0 recall events for this product code

See all →

No recalls on file for this product code.