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Apparatus, Electrophoresis, For Clinical Use

FDA product code JJN · Class 1 · Clinical Chemistry

3
Registered devices
2
Adverse events
1
Recalls
34
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2017-05-15Perkinelmer Life Sciences, Inc.Potential for electric shock in the case of a failure to install the grommets, supplied with the system.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.