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Electrosurgical Electrode Kit

FDA product code NWI · Class 2 · Gastroenterology, Urology

2
Registered devices
2
Adverse events
1
Recalls
0
510(k) clearances

Devices with this code

Medline Industries, Inc. — MEDLINE INDUSTRIES, INC.NA — US Endoscopy

Recent recalls

DateFirmReason
2004-09-24Datascope CorpSoftware anomaly where the variable heart rates may be displayed inaccurately or intermittent 'dashes' may be displayed when the patient's heart rate is derived

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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.