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Urethrometer

FDA product code FBR · Class 1 · Gastroenterology, Urology

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Registered devices
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Adverse events
1
Recalls
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510(k) clearances

Recent recalls

DateFirmReason
2022-02-22Busse Hospital Disposables, Inc.Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a dru

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