JJNClass I

Apparatus, Electrophoresis, For Clinical Use

Clinical Chemistry · 21 CFR 862.2485

MDR events2All time

Recalls1All time

Registered firms13Currently listed

510(k) clearances34All time

Recent MDR events

2 adverse event reports on file

Event type breakdown

Malfunction2

Most-reported manufacturers

Sebia Inc1 Sebia Inc.1

Recalls

1 recall events for this product code

Perkinelmer Life Sciences, Inc.
TerminatedMay 22, 2017
Multiphor II Electrophoresis System
Potential for electric shock in the case of a failure to install the grommets, supplied with the system.
Z-2685-2017 · View FDA record ↗

Registered firms

13 firms currently registered for this product code

510(k) clearances

34 clearances for this product code